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. 2017 Jul 7;8:94. doi: 10.3389/fgene.2017.00094

Table 1.

Read pre-processing strategies used in this study.

Pre-processing strategy Quality trimming∗∗ Merging of overlapped pairs∗∗∗ PCR de-duplication∗∗∗∗
Lax Lead:Q20, Trail:Q15, Wlen:10,Q15 No No
Medium Lead:Q25, Trail:Q20, Wlen:15,Q20 No No
Hard Lead:Q25, Trail:Q25, Wlen:20,Q25 No No
Lax + Ovl Lead:Q20, Trail:Q15, Wlen:10,Q15 Min Ovl 15 bp No
Medium + Ovl Lead:Q25, Trail:Q20, Wlen:15,Q20 Min Ovl 15 bp No
Hard + Ovl Lead:Q25, Trail:Q25, Wlen:20,Q25 Min Ovl 15 bp No
Lax + PCR Lead:Q20, Trail:Q15, Wlen:10,Q15 No MDR = 0.03
Medium + PCR Lead:Q25, Trail:Q20, Wlen:15,Q20 No MDR = 0.03
Hard + PCR Lead:Q25, Trail:Q25, Wlen:20,Q25 No MDR = 0.03

From left to right, columns contain:

Description of the strategy, as described in main text and figures.

∗∗Trimmomatic parameters for quality trimming. Q, quality score cut-off; Wlen, length of the window for sliding window operations.

∗∗∗Pear parameters for read merging. Min Ovl, minimum overlap required for merging of read pairs.

∗∗∗∗MarkDuplicates parameters for PCR de-duplication. MDR (MAX DIFF RATE), overall mismatch rate for non-duplicated reads.