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Table 3 Mapping metrics for assemblies

From: Single molecule sequencing and genome assembly of a clinical specimen of Loa loa,the causative agent of loiasis

Assembler

Sequencing data

FR reads

RF reads

Tandem

Median insert Size ± Abs. Dev.

Mean insert Size ± St. Dev.

CA

Illumina MiSeq

7,163,609

690

739

470 ± 45

480 ± 72

MaSurCA

Illumina MiSeq

7,315,963

340

137

469 ± 44

478 ± 71

CLCBio

Illumina MiSeq

6,917,178

103

29

466 ± 44

475 ± 72

CA

Illumina-corrected PacBio reads

7,292,995

694

298

470 ± 44

479 ± 71

CA

Illumina- and 454-corrected PacBio reads

7,459,123

600

288

470 ± 44

480 ± 71

HGAP2

PacBio reads

7,544,255

696

826

471 ± 45

480 ± 71

HGAP2 with trimming

PacBio reads

7,564,549

697

827

471 ± 45

480 ± 71

  1. This table provides the statistics about the mapping of all of the Illumina read pairs against all of the contigs generated by various combinations of assemblers and data sets as assessed by PICARD. The statistics reported include the number of FR reads, the number of RF reads, the number of tandem reads, the median insert ± on absolute deviation, and the mean insert size ± one absolute deviation.