Exploring the gonad transcriptome of two extreme male pigs with RNA-seq
© Esteve-Codina et al; licensee BioMed Central Ltd. 2011
Received: 13 June 2011
Accepted: 8 November 2011
Published: 8 November 2011
Although RNA-seq greatly advances our understanding of complex transcriptome landscapes, such as those found in mammals, complete RNA-seq studies in livestock and in particular in the pig are still lacking. Here, we used high-throughput RNA sequencing to gain insight into the characterization of the poly-A RNA fraction expressed in pig male gonads. An expression analysis comparing different mapping approaches and detection of allele specific expression is also discussed in this study.
By sequencing testicle mRNA of two phenotypically extreme pigs, one Iberian and one Large White, we identified hundreds of unannotated protein-coding genes (PcGs) in intergenic regions, some of them presenting orthology with closely related species. Interestingly, we also detected 2047 putative long non-coding RNA (lncRNA), including 469 with human homologues. Two methods, DEGseq and Cufflinks, were used for analyzing expression. DEGseq identified 15% less expressed genes than Cufflinks, because DEGseq utilizes only unambiguously mapped reads. Moreover, a large fraction of the transcriptome is made up of transposable elements (14500 elements encountered), as has been reported in previous studies. Gene expression results between microarray and RNA-seq technologies were relatively well correlated (r = 0.71 across individuals). Differentially expressed genes between Large White and Iberian showed a significant overrepresentation of gamete production and lipid metabolism gene ontology categories. Finally, allelic imbalance was detected in ~ 4% of heterozygous sites.
RNA-seq is a powerful tool to gain insight into complex transcriptomes. In addition to uncovering many unnanotated genes, our study allowed us to determine that a considerable fraction is made up of long non-coding transcripts and transposable elements. Their biological roles remain to be determined in future studies. In terms of differences in expression between Large White and Iberian pigs, these were largest for genes involved in spermatogenesis and lipid metabolism, which is consistent with phenotypic extreme differences in prolificacy and fat deposition between these two breeds.
Understanding the mammal transcriptome architecture has proven to be a complex task [1–4]. The advent of high throughput sequencing technologies, such as RNA-seq, has, yet, substantially improved our comprehension of its structure and expression patterns. By deep sequencing the poly-A RNA fraction, it is possible not only to better characterize isoforms from known genes (e.g., identifying novel exons, new transcription start sites and alternative polyadenylation sites), but also to improve the annotation by discovering novel predicted coding genes and polyadenylated processed transcripts such as long intergenic non-coding RNAs . Although several surveys of the transcriptome from different tissues have been conducted in humans and model species [6–17] our knowledge of livestock species remains limited. For instance, the relation between extreme phenotypic differences and their transcriptome patterns is poorly studied. The transcriptome of livestock species is, by comparison to model species, much less known despite its economic and social interest.
In this study, we used high-throughput transcriptome sequencing in two pigs from extreme breeds. Our aim was to discover and characterize novel expressed transcripts and to identify differentially expressed genes that may explain some of the phenotypic variation. We sequenced the male gonad transcriptome of a Large White and an Iberian pig, two highly divergent phenotypic breeds in terms of production traits, e.g., growth, fatness and reproductive performance. To limit the effect of enviromental influences on gene expression pattern, both pigs were housed and fed with the same conditions and were prepubescent at slaughter time. Furthermore we compared the results obtained with RNA-seq with microarray data published in a previous study . Finally, we also identified polymorphic sites and genes that potentially showed allele specific expression.
Results and Discussion
We obtained about 60 M of 50 bp paired-end reads from one lane of an Illumina GAIIx machine, about 30 M was derived from each sample (Data are archived at NCBI Sequence Read Archive (SRA) under Accession SRP008516). After ambiguous mapping (allowing for multi-hits) with Tophat  a total of 20 M reads for each sample were mapped against the reference pig genome (assembly 9), although only 10 M were classified as proper pairs. The rest (4 M) fell into either one of these categories: reads without a mapped mate pair, mate is mapped on the same strand or mates overlap. The most likely explanations of the large amount of improperly mapped reads are the poor quality of the current pig genome assembly and the stringency of the version of Tophat used here, as this version does not allow gaps for the mapping. In addition, any situation where the distance between the mates is larger than the confidence interval of the insert size distribution, could be interpreted as trans-splicing events , structural variants or simply mapping artifacts . The total number fragments mapped with unambiguous mapping (1 hit per read) were 14 M for each sample; out of these, 7 M were classified as proper pairs. A comparison between ambiguous versus unambiguous mapping results obtained with Tophat is shown in Additional file 1.
Annotation of reads and transcripts assembly
Summary of reads' annotation
5' Upstream or 3'Downstream
A total of 4,124 novel transcripts (the real number of transcript units may be smaller, as less abundant transcripts receive less complete sequencing coverage resulting in numerous transfrags) were identified in intergenic regions (see methods). To investigate which of these transcripts actually encode a protein, we used Augustus  and found 714 novel putative proteins. We identified homologous DNA sequences (see methods) in Bos taurus and Homo sapiens genomes for most (413) of these novel proteins: 362 were orthologs with both cow and human, 20 with human only and 31 with the cow genome only. This result is consistent with Bos taurus being closer to Sus scrofa than human . Interestingly, when we looked for homologous DNA regions within the Sus scrofa genome, 53 paralogous regions were detected (51 duplications and 2 present in three copies).
To find out whether the predicted proteins from the homologous regions were already annotated, we ran BLASTP against the Homo sapiens, Bos taurus and Sus scrofa protein databases (http://www.ensembl.org/info/data/ftp/index.html). Overall, we identified 38 novel computationally predicted and 344 known proteins for the human, 15 novel predicted and 378 known proteins for the cow and 653 novel predicted and 89 known proteins for the pig. The novel computationally predicted proteins found in the pig are now experimentally confirmed by RNA-seq. See Additional file 2 for the coordinates of orthologous and paralogous genes.
As many previous studies reported high activity of transposable elements (TE) in germlines [24–27], we ran RepeatMasker to identify repetitive elements in the pig genome and in the transcriptome of the testicles. The fraction of transposable elements expressed in male gonads (SINEs, LINEs, LTR and DNA elements), compared to the total number detected in the pig genome, is less than 3%. However, approximately 20% of the expressed transcripts units harbor at least 1 transposable element (8% of the bp sequenced). The type of TE being more active in both breeds, in terms of number of elements expressed divided by the total number present in the genome, is DNA transposons, but accounting just for the number of elements expressed is SINE family for Large White and the LINE family for Iberian. LINE1 elements also have been reported to contribute to the transcriptome in human somatic cells . It is interesting to mention that 16% of protein-coding transcripts contain transposable elements in their sequence and they are transcribed in the same transcript unit. Apart from these interspersed repeats, hundreds of small RNA (tRNA, snRNA and rRNA) and thousands of simple and low complexity repeats were also identified in the transcriptome. The presence of non-polyadenylated RNA could be a remaining contamination as they are highly expressed molecules and difficult to remove completely. Another possible explanation is the presence of small functional RNAs embedded in the introns of polyadenylated molecules of pre-mRNA [29, 30]. Detailed results of the repetitive elements detection with Repeatmasker are shown in Additional file 3a and 3b.
In order to define a set of putative lncRNAs in the pig transcriptome, we applied several filtering criteria. Using the procedure in  for the definition of lncRNA in humans, we excluded all transcripts mapping within 1 kb of an annotated protein-coding gene in the pig genome. This makes it less likely to consider the 5' or the 3' UTR of a protein-coding gene as a non-coding RNA. Yet, this filtering may not be stringent enough when dealing with insufficiently annotated genomes. For that reason, we further refined our analysis by excluding all transcripts coding for a complete proteins (according to Augustus). A third filter was applied by removing all transcripts having a hit against NR (BlastX), against Pfam (RPS-Blast) or against Rfam  (web-site batch search). The final filter was applied mapping all the resulting transcripts onto the human genome (the best annotated mammalian genome), and removing any transcript strongly overlapping with a protein-coding gene. The result is a dataset made of 2047 transcripts and referred in the rest of this text as the lncRNAs.
It is worth mentioning that the transcripts thus identified have a gene structure significantly different from their human counterparts. 97% are single exon genes and 2.5% bi-exonic, a figure significantly different from human where a much higher portion is bi-exonic. This finding may simply reflect insufficient coverage in the RNA-seq experiment resulting in truncated cufflinks models and thus should not be taken, so far, as strong evidence of distinct lncRNA organization between species.
It is in agreement with our observation that the lncRNA we observe in pig are roughly half the size of those reported in human (456 vs 925). As a consequence, the number of independent transcripts reported here is quite likely to be an over estimation.
Gene expression analysis
In total, 12,816 annotated genes were expressed in gonads. Less than 1% of these genes were expressed more than 10000 FPKM; around 5% were expressed between 1000 -10000 FPKM, 50% between 10-1000 FPKM, 40% between 10-100 FPKM and 3% between 1-10 FPKM (Additional file 4). The rest were expressed below 1 FPKM. The maximum expression level of an annotated gene was 61,000 and 73,000 FPKM in Large White and Iberian, respectively. The gene ontologies of the 100 most expressed genes (mainly ribosomal proteins and heat-shock proteins) in both samples were related with transcription and translation, protein folding, lipid and cholesterol metabolism (apoproteins), induction of apoptosis and response to stress. These results are consistent with those observed in other mammalian species with RNA-seq .
The correlation of gene expression levels between both samples (Large White vs. Iberian) was very high (r = 0.85), which suggests that a large fraction of the transcriptome is conserved across individuals. This is consistent with our previous results which showed that the largest source of variability was tissue rather than sex or breed .
We also compared the RNA-seq expression results with Affymetrix microarray data obtained in a previous study . As many microarray probes may map to the same gene, the average probe value per gene was calculated. A total of 9,112 Ensembl ID genes could be retrieved from microarray probes data for RNA-seq comparisons. The correlation between the individual microarray signal intensity difference and the log2 of the fold change from RNAseq was quite high (r = 0.71, see Figure 3b). From the microarray study, we also had a Bayesian standardized breed score (z-score) available for each gene. When comparing the microarray breed z-score and the log2 of the fold change in RNA-seq, the correlation was also moderately high (Pearson correlation r = 0.46, see Figure 3c).
Differential expression analysis
Expression differences of coding and non-coding genes
The GC content median of the coding genes (annotated 0.46 and novel 0.47) was the same but higher than the lncRNA (0.42) and transcripts harboring at least one TE (0.42) because coding genes tend to be rich in GC . Important to notice is the fact that GC content of annotated genes differs depending on whether we provide to Cufflinks the reference gene annotations (Figure 5c) or not (Figure 5d). In the former, the GC content is much higher (0.53) than the latter (0.46), pointing to a possible bias towards AT during Illumina library preparation and sequencing workflow. Recently, a new amplification protocol has been published that solves this problem .
Non synonymous coding
Non synonymous coding
Within non coding gene
Allele specific expression
Several SNP with significant ASE are located contiguously within intergenic regions, suggesting the presence of putative functional units not yet annotated in the pig genome. There were not many genes with ASE shared between the two samples, likely due to different genotypes at the regulatory motif of the two breeds. There were only 22 common SNPs exhibiting ASE in both animals, but in three of the SNPs we observed over expression of different alleles in each breed. Logically, these results should be taken as statistical evidence, genotyping or sequencing the cis-regulatory motives and linkage disequilibrium information are, however, needed to confirm whether these SNPs show genuine ASE.
We present the first, to our knowledge, comprehensive exploration of the pig gonad transcriptome carried out with RNA-seq, a technology that offers critical advantages over microarray. Importantly, RNA-seq allows us to improve dramatically the annotation of the species and the discovery of new splicing events. Here, we have confirmed that a large part of the transcription effort in the cell is spent on TE sequences. A recent RNA-seq study in human and primate brain transcriptomes also found high proportion of reads mapping to repetitive elements, mainly from the Alu family . Previous works in mice also indicated high expression of TE in germlines. The number of TE is probably an over-estimation as we did an ambiguous mapping reporting only the best alignments. On the other side, Cufflinks down weights the expression level taking into account mapping uncertainty .
Unfortunately, we also confirm that current porcine annotation is incomplete, as evidenced by read mapping annotation: more than 50% of the fragments do not map to annotated exons. The fact that many reads map to introns could be explained either by intron retention (new isoforms) or pre-mRNA presence. Reads mapping outside the boundaries of annotated genes could be explained either by polymerase run-on fragments or a bad annotation of the gene endings. Many intergenic reads have been mapped to putative novel coding transcripts, some of them presenting orthology with related species. The poor status of the annotation is confirmed by the presence of 104 highly conserved transcripts, that would have been annotated as lncRNAs if we had only considered the pig annotation, but whose homologues in human show a perfect overlap with protein-coding genes.
Given that we had previously analyzed the transcriptome of a wider collection of pig and tissues with Affymetrix microarrays , we were able to compare both technologies. The correlation within individuals was rather high (r = 0.71) and comparable to other reported studies [6, 41–44]. Furthermore, the correlation of expression between Iberian and Large White obtained with microarray (employing all animals) and the individuals (obtained with RNAseq) was also moderately high (r = 0.46), suggesting that transcriptome patterns are relatively stable. Among the most differentially expressed genes, those involved in spermatogenesis and lipid metabolism are over-represented, which may be a result of targeted tissue selection. It is noteworthy that Large White and Iberian breeds are phenotypically extreme for both reproduction and fat deposition traits so these data would suggest a correlated effect on the regulation of genes involved in these traits.
In general, Cufflinks has a better performance to map fragments to genes or isoforms that are physically overlapping or very similar in sequence, as it uses a statistical model to deal with multiply mapping fragments. DEGseq works with uniquely mapped reads, thus underestimating gene expression levels of homologous genes but also discarding those reads belonging to two overlapping genes; a bias in expression level is thus introduced in these cases. The algorithm behind Cufflinks is rather naïve, though. Recently, new approaches that implement improved algorithms to deal with ambiguously mapped reads data and avoid bias in downstream analysis have been published [45, 46].
Although not the main purpose of the work, we also found a lower rate of heterozygosity in Iberian than in the Large White animal, in agreement with the fact that Iberian pigs are normally inbred. Finally, we also explored ASE, a topic that has received a renewed interest recently. In this study, ~ 4% of the segregating SNP presented allelic imbalance. From these, around 40% were located inside annotated genes, the rest were located in blocks in intergenic regions, pointing to putative functional transcripts. To be able to confirm ASE, more animals should be tested because the majority of the SNPs with ASE were not common between Large White and Iberian pigs.
We provide a complete survey of the pig male gonad transcriptome and identified many novel elements. However, to further improve the annotation of the pig genome, a large effort from the community will be necessary by sequencing more tissues at different developmental stages. In order to detect novel splicing events and to reconstruct novel isoforms, RNA-seq studies with very high coverage are required. Here, we also have shed some light on the dark matter of the transcriptome; in particular, we remark the discovery of novel long non-coding transcripts and the fact that TE expression seems to take a large fraction of the transcriptome. Their precise roles need to be elucidated in future studies. We also show that correlation between microarray and RNAseq expression data are reasonably high (linear correlation r = 0.71). Finally, Large White and Iberian pigs seem to have diverged most for genes involved in spermatogenesis and lipid metabolism, not only in terms of gene expression but also phenotypically. Interestingly, it is well known that genes related to gametogenesis are subject often to a positive selection rate [47, 48]. More work is required to investigate whether the differences in expression in these genes are adaptive.
Animal material is fully described in . The two animals were housed and slaughtered simultaneously. Animals were prepubescent, three months of age, and weights were 45.0 and 30.1 kg for Large White and Iberian animals, respectively.
Total RNA from gonads was extracted as described in . Briefly, Total RNA was extracted from 100 mg tissue using the RiboPure™ kit (Ambion, Austin, USA). RNA integrity was assessed by Agilent Bioanalyser 2100 and RNA Nano 6000 Labchip kit (Agilent Technologies, Palo Alto, USA). Due to high variation in concentrations of the total RNA obtained in different tissues, all samples were concentrated and cleaned using the RNAeasy MiniElute Cleanup kit (Qiagen, Basel, Switzerland) obtaining final concentrations between 500 and 1000 ng/μl. Sequencing libraries were produced using the Illumina mRNA-Seq sample preparation kit, following the manufacturer's instructions. Briefly, 4 μg of total RNA were used as input for poly-A+ selection, followed by metal-catalyzed fragmentation of the selected mRNA (peak of size distribution at approx. 240 nt). After reverse transcription to cDNA using random hexamer primers, we performed end-repair and A-tailing of the double stranded cDNA. Large White and Iberian cDNA were ligated to indexed pairs of adapters, see Additional file 6. The cDNA was size selected on a 2% agarose gel, and fragments corresponding to an insert size of 237 nucleotides were excised from the gel. The DNA was recovered from the gel slice using QIAquick gel extraction kit (Qiagen). Therafter, the libraries were amplified in 15 cycles of PCR using primers Illumina 1.0 and Illumina 2.0. The libraries were quantified using Taqman, and pooled at a concentration of 10 pM. We performed paired-end sequencing of the libraries on the Genome Analyzer IIx using Illumina v4 sequencing chemistry.
S-MART (http://urgi.versailles.inra.fr/Tools/S-MART) was used to count the number of reads mapping to exons, introns and 1 kb upstream/downstream of the annotated genes. A minimum overlapping of 1 nucleotide was chosen to declare an overlap.
Mapping, Assembling and Quantifying
Reads were mapped against the pig reference genome (assembly9) with Tophat v.1.0.14  using the following settings: maximum of 40 hits per read (reporting best alignments), expected mean inner distance between mate pairs of 137 and a standard deviation for the distribution on inner distances between mate pairs of 100. For unambiguous mapping of the reads, the maximum alignments per read were set to 1. Sequence statistics were analyzed with FASTQC (http://www.bioinformatics.bbsrc.ac.uk/projects/fastqc). Base sequence qualities and proportion of bases per cycle are shown in Additional files 7a and 7b. A decrease in base quality is observed towards the end of the sequence and there is a bias in nucleotide content in the first 10 cycles of the reads due to the random hexamer primer library preparation approach . Recently, a new statistical approach has been proposed to solve this bias . Transcripts were assembled and quantified by Cufflinks v.0.9.0 . To improve the robustness of the differential expression estimates the quartile normalization was used and the contribution of the top 25 percent most highly expressed genes was excluded (-N option). The minimum alignment count per locus was set to 20 (-c option).
Intergenic expressed regions not yet annotated in the pig genome were extracted with Cuffcompare  and custom Python and R scripts. Only those regions expressed in both samples were considered for a conservative approach. To identify putative coding transcripts, we run Augustus  providing exon boundaries and allowing only complete proteins translations from the forward strand.
Transposable element analysis
We run RepeatMasker (http://www.repeatmasker.org/) with options 'quick search' and species 'pig' to identify repetitive and transposable elements (TE) in pig genome and male gonads transcriptome. We used RepeatMasker version open-3.2.9, rmblastn version (1.2) 2.2.23 and RepBase update 20090604.
All the transcripts not overlapping with pig protein-coding genes and falling at least 1 kb away from the closest protein annotation were considered for our analysis. A series of filtering steps were then implemented. The first one consisted in selecting the transcripts for which Augustus returned no (or just partial) coding potential. BlastX (NCBI Package version 2.2.25) was then used to search all possible translational products (the six possible reading frames) of each transcript against the NCBI non-redundant protein database (last update 05/29/2011). All the transcript queries that matched a known protein with an expectation value lower than 10-5 were discarded. Likewise, RPS-Blast (NCBI Package version 2.2.25) was used to search the possible translational products of each transcript against a database of Pfam profiles  and the transcripts returning an expectation value lower than 10-5 were removed. In order to filter the transcripts belonging to known classes of RNAs (snoRNAs, tRNAs, etc...), all the sequences were sought against Rfam (Release 10.0) using the Rfam searching facility available at: http://rfam.sanger.ac.uk/search#tabview=tab0.
Finally the remaining transcripts were remapped against the human genome and the homologous positions were intersected with protein-coding gene annotations (GENCODE version 3c). The screening was performed using a combination of BlastN and exonerate (as described in the screening pipeline in the methods). The transcripts whose human homologue resulted to be fully included in protein-coding exons were removed.
The screening pipeline was composed by three phases. The first consisted in seeking each query against the target genomes with a version of BlastN optimized for ncRNAs discovery . Secondly, using exonerate each query was realigned versus the genomic regions pointed by Blast. For each query and for each genome was kept just the best hit that was successfully realigned. The exonerate alignments spanning for at least the 70% of the pig queries were retained. Finally, each query was compared versus all the putative discovered homologs by realigning the transcripts sequences with T-Coffee  and measuring the query/homolog pairwise similarity.
Differential expression (DE) analysis
To test DE with unambiguous mapping data DEGseq was used . MA plot-based method (where M is the log ratio of the counts between two experimental conditions for gene g, and A is the two group average of the log concentrations of the gene) with a random sampling method (MARS) was selected. To count the number of fragments that uniquely map to an exon, HTseq-count was used with 'union' as overlapping mode, 'gene' as feature and not strand-specific. A locus was considered as expressed if it had a minimum count of 40 fragments (summing the reads in both samples). From a total of 9 M unambiguously mapped reads for each library, 4.5 M of reads felt in the category of 'no_feature' (no annotation provided). The software discarded reads mapping to two overlapping genes (20,000 reads). Cuffdiff  was used to test DE using same options as discussed above for ambiguous mapping data.
where PT, PB and PS stand for the probeset × tissue, probeset × breed and probeset × sex interactions, respectively. The Bayesian breed z-score for the g-th probeset is defined as z g = E(PBg|y)/SD(PBg|y), where E(PBgj|y) and SD(PBgj|y) are the expected and SD values of the posterior distribution of PB, respectively .
Gene ontology analysis
Parental gene ontology enrichment analysis was performed with the QuickGO browser (http://www.ebi.ac.uk/QuickGO/) using a GOSlim extracted from the AmiGO browser (http://amigo.geneontology.org/cgi-bin/amigo/go.cgi) and made up of 23 parental pig GO: biological regulation, cellular process, metabolic process, multicellular organismal process, developmental process, signaling, localization, response to stimulus, immune system process, cellular component organization, reproduction, biological adhesion, cellular component biogenesis, death, locomotion, multi-organism process, growth, pigmentation, rhythmic process, viral reproduction and cell killing. Expected and observed GO percentages were compared with a Fisher's exact test as implemented in R. To test for an enrichment of specific ontology categories, we simply computed a two-sided t-test assuming a normal distribution for number of counts. The children gene ontology enrichment and KEGG pathway analyses were performed with the DAVID database (http://david.abcc.ncifcrf.gov/). Prior to GO analysis, the pig gene IDs were converted to human gene IDs with Biomart (http://www.biomart.org/) as the database had poor pig Ensembl annotations. The list of differentially expressed genes (intersection of Cufflinks and microarray breed effects) was compared against total expressed genes in male gonads (background).
S NPs were identified from unambiguously mapped reads using Samtools (http://samtools.sourceforge.net/). The minimum SNP quality was 10 and the minimum read depth was set to 3 × for fixed SNP with respect to the reference and 4 × for segregating SNP. As many false SNP were located at the splice sites due to the difficulties of alignments near indels (splicing sites), they were removed from the final set. Annotation of the SNP was made with custom Perl scripts using the Ensembl APIs.
Allele specific expression
where Be() is a beta distribution; B(), a binomial; n is the number of reads for that SNP; n a , the number of reads pertaining to one arbitrary allele, and α and β are hyperparameters. The data was fitted using an empirical Bayesian approach such that the mean and variance of Be(α, β) were those observed in the real data. The obtained α and β were 4.99 and 3.84 in Large White and 6.38 and 6.20 in the Iberian data, respectively. ASE was considered when the 95% Highest Density Region (HDR) did not include p = 0.5. HDR was computed with function "HDIofICDF.R" in R (http://www.indiana.edu/~kruschke/DoingBayesianDataAnalysis/Programs/HDIofICDF.R).
Long non-coding RNA
Fragments Per Kilobase of exon model per Million mapped fragments
Allele specific expression
Peroxisome proliferator-activated receptor
Kyoto Encyclopedia of genes and genomes
Single nucleotide polymorphism
Application programming interface
Part of this work was done during a visit of AEC to Institut für Populationsgenetik, (Vienna), and we thank C. Schlötterer for hospitality. Thanks to J. Estellé for help with annotating SNPs. Sequencing was carried out at the ultra sequencing service unit of Center for Genomic Regulation (http://seq.crg.es/main/bin/view/Home/WebHome). AEC is recipient of a FPI PhD fellowship from Ministry of Education, Spain. Work funded by AGL2010-14822 grant to MPE and by a Consolider grant from Spanish Ministry of Research, CSD2007-00036 "Centre for Research in Agrigenomics". RK and NP were supported by the FWF grant P19467 awarded to C. Schlötterer. CN and GB were co-funded by the Plan Nacional BFU2008-00419, the European Commission, within the 7th Framework Programme, Grant Agreement KBBE-2A-222664 ("Quantomics"), the La Caixa PhD program and the Centre de Regulació Genomica.
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