Question: processing amplicon seq data from miseq
0
gravatar for sc222
21 months ago by
sc2220
sc2220 wrote:

I have .fastq files from a targeted amplicon seq run on MiSeq using Illumina library prep workflow. How do I process it so that I get the targeted sequences? What is the pipeline to use for processing amplicon sequencing?thanks in advance.

next-gen • 860 views
ADD COMMENTlink modified 21 months ago by Vitis2.4k • written 21 months ago by sc2220

FYI: This is crossposted on stackexchange.

ADD REPLYlink written 21 months ago by finswimmer14k
1
gravatar for Vitis
21 months ago by
Vitis2.4k
New York
Vitis2.4k wrote:

Based on amplicon size, you may either map the paired-end reads or generate the combined reads (from the pairs) before mapping to the reference genome. It should be straightforward with BWA (or BWA MEM). How you deal with the alignments largely depends on the purpose of the experiment, genotyping or sequence assembly, could all start from the BAM files.

ADD COMMENTlink written 21 months ago by Vitis2.4k
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