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. 2013 May 6;8(5):e61479. doi: 10.1371/journal.pone.0061479

Table 2. Assembly statistics and BLAST results against nr for the G. bimaculatus de novo transcriptome assembly.

Parameter1 Value
# bp Raw reads 1,483,726,666
Maximum raw read length 803
Minimum raw read length 13
Median raw read length 364
Maximum assembled read length 771
Minimum assembled read length 20
Median assembled read length 358
# Isogroups2 (“genes”) 16,456
Mean # isotigs per isogroup 1.2
# Isotigs 21,512
Maximum isotig length 10,865
Minimum isotig length 57
Median isotig length 1,054.5
# Isotigs with BLAST hit against nr 3, E-value cutoff e-10 (% of all isotigs) 11,135 (51.8%)
# Isotigs with BLAST hit against nr, E-value cutoff e-5 (% of all isotigs) 11,943 (55.5%)
Mean # contigs per isotig 1.7
# Singletons 120,805
Maximum singleton length 620
Minimum singleton length 50
Median singleton length 250.5
# Singletons with BLAST hit against nr, E-value cutoff e-10 (% of all singletons) 7,914 (6.6%)
# Singletons with BLAST hit against nr, E-value cutoff e-5 (% of all singletons) 10,815 (9.0%)
# Non-redundant assembly products (NRAP) 142,317
# NRAP with BLAST hit against nr, E-value cutoff e-10 (% of all NRAP) 19,049 (13.4%)
# NRAP with BLAST hit against nr, E-value cutoff e-5 (% of all NRAP) 22,758 (16.0%)
Total # BLAST hits4 (nr) 22,758
Average coverage/bp 51.3
1

Values for number of raw reads, number and % of raw reads assembled (passed quality filters described in main text), number of contigs, isotig N50, % of singletons, total number of assembly products, and number of unique BLAST hits against nr, are shown in Table 1.

2

Because isogroups are collections of isotigs that are hypothesized to originate from the same gene, they do not comprise a single sequence and so cannot be mapped to nr using BLAST.

3

nr = NCBI non-redundant database.

4

For BLAST against nr the E-value cutoff was 1e-5. For breakdown of BLAST hits among different classes of assembly sequences, see Table 3.