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  • vishnuamaram
    replied
    Hey nxtgenkid10

    if your data is paired end, this is the way you should go.

    1) bwa index ref.fa = index your ref. genome.

    2) bwa aln ref.fa short_read.fq > aln_sa.sai = get sai files for both reads, say read1 & read2.

    then do

    3) bwa sampe ref.fa aln_sa1.sai aln_sa2.sai read1.fq read2.fq > aln-pe.sam

    Leave a comment:


  • dpryan
    replied
    Have you read the BWA manual page?

    Leave a comment:


  • nxtgenkid10
    started a topic bwa reference genome alignment

    bwa reference genome alignment

    I like to know how to run bwa to align my pe reads to the reference genome

    first i tried to create the reference of the bac genome bwa index -a is /Reference/ref.fa

    I tried the following command to align
    bwa sampe /DATA/Read1.fastq /DATA/Read2.fastq

    But i couldn t find an option to put my reference sequence for alignment

    and should i use bwa aln also if so y and how?

    Thanks

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