Changes between Version 63 and Version 64 of SOPs/qc_shortReads
- Timestamp:
- 08/19/24 12:43:07 (5 months ago)
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SOPs/qc_shortReads
v63 v64 306 306 307 307 During quality control, if low-quality reads have been removed for any reason, some reads may not have a paired end at the other end. This can cause problems with mapping programs. 308 308 * '''Method 1''': 309 309 Sample command: 310 310 … … 318 318 319 319 The *common.out reads should be used for paired-read mapping. 320 321 * '''Method 2''': 322 For fastq.gz files use the seqkit instead 323 [https://bioinf.shenwei.me/seqkit/usage/ seqkit] 324 {{{ 325 seqkit pair -1 sequence.1_1.filt.fq.gz -2 sequence.1_2.fil.fq.gz # fastq inputs 326 }}} 327 320 328 321 329 == Select a subset of reads by read ID ==