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Table 1 Benchmarks of four programs with three multiplex amplicon sequencing datasets. ‘Trimmed Reads’ indicates the reads that had any number of bases removed by the program. ‘Precisely Trimmed Reads’ indicates the reads whose primer sequences were precisely trimmed. K: the number of nucleotides for “k-mer” algorithm. Err: the number or percentage of allowed mismatches for primer searching. See Additional file 1 for the detailed parameters to run each of these programs

From: pTrimmer: An efficient tool to trim primers of multiplex deep sequencing data

Sample (No. of reads)

 

Alientrimmer

Cutadapt

cutPrimers

 

Parameter

1 thread, K = 9, err = 3

8 threads, err = 10%

8 threads, err = 3

2 threads, k = 9, err = 3

CfDNA1 (11,498,560)

Time of

1137

108,918

2224

35

CfDNA2 (16,694,386)

Running (s)

2511

170,920

3646

47

CfDNA3 (36,119,764)

 

6099

349,789

7772

62

CfDNA1 (11,498,560)

No. of

2,228,698 (19.28)

11,392,006 (99.07)

8,733,142 (75.95)

10,973,548 (95.43)

CfDNA2 (16,694,386)

Trimmed Reads (%)

3,193,584 (19.13)

16,633,850 (99.64)

12,481,890 (74.77)

16,023,158 (95.98)

CfDNA3 (36,119,764)

 

5,680,392 (15.73)

35,921,534 (99.45)

24,460,516 (67.72)

32,314,848 (89.47)

CfDNA1 (11,498,560)

No. of

81,143 (0.71)

389,526 (3.39)

7,752,109 (67.42)

10,908,534 (94.87)

CfDNA2 (16,694,386)

Precisely Trimmed Reads (%)

134,647 (0.81)

516,377 (3.09)

11,130,147 (66.67)

5,905,037 (95.27)

CfDNA3 (36,119,764)

 

236,252 (0.65)

1,003,057 (2.78)

21,581,726 (59.75)

12,024,840 (88.66)