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Correction to: SALP, a new single-stranded DNA library preparation method especially useful for the high-throughput characterization of chromatin openness states
BMC Genomics volume 19, Article number: 327 (2018)
- The original article was published in BMC Genomics 2018 19:143
After publication of the original article  the authors noted that the additional files had not been uploaded correctly.
While the legends are correctly cited, the figures themselves are incorrect.
The correct order of additional files follows below:
|Original Additional Files||Correct Additional Files|
|Additional File 1||Additional File 10|
|Additional File 2||Additional File 11|
|Additional File 3||Additional File 1|
|Additional File 4||Additional File 2|
|Additional File 5||Additional File 3|
|Additional File 6||Additional File 4|
|Additional File 7||Additional File 5|
|Additional File 8||Additional File 6|
|Additional File 9||Additional File 7|
|Additional File 10||Additional File 8|
|Additional File 11||Additional File 9|
A full list of the correct corresponding files and their legends are included with this Correction.
The publisher apologises for this error.
Wu J, Dai W, Wu L, Wang J. SALP, a new single-stranded DNA library preparation method especially useful for the high-throughput characterization of chromatin openness states. BMC Genomics. 2018;19:143. https://doi.org/10.1186/s12864-018-4530-3.
Table S1. Oligonucleotides used as adaptors and PCR primers. (DOCX 15 kb)
Table S2. Barcodes on Barcoded Tn5 adaptors for labeling different cell samples. (DOCX 14 kb)
Figure S1. Validation of SALP method. (DOCX 309 kb)
Cloning sequencing. (DOCX 21 kb)
Figure S2. The structure of SALP library. (DOCX 68 kb)
Figure S3. Verification of the ligation efficiency of SSA adaptors. (DOCX 187 kb)
Table S3. Reads from a lane of Illumina Hiseq X Ten sequencing. (DOCX 15 kb)
Figure S4. Comparison of fold enrichment of two types of GM12878 SALP-seq peaks. (DOCX 45 kb)
Figure S5. Construction of NGS library of gDNAs sheared by sonication and restriction endonuclease digestion with SALP method. (DOCX 295 kb)
Figure S6. Comparison of the distribution of Hind III digestion library reads density and Hind III restriction sites through the whole genome. (DOCX 444 kb)
Figure S7. Reads distribution of sonication library. (DOCX 395 kb)
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Cite this article
Wu, J., Dai, W., Wu, L. et al. Correction to: SALP, a new single-stranded DNA library preparation method especially useful for the high-throughput characterization of chromatin openness states. BMC Genomics 19, 327 (2018). https://doi.org/10.1186/s12864-018-4688-8