Hi guys,
Glad to find this place.
Now I'm trying to use 50X pacbio reads for human genome re-sequencing analysis, like...
3 results in 0.0022 seconds.
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snp calling by Pacbio reads
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best way to re-sequence a few Mb of genomic sequences
Hi,
If I want to re-sequence a known part of the chromosome (we know the reference genome sequence) of ~1Mb to find the possible mutations (SNP... -
Dindel empty variant result file
I'm running dindel's first stage analysis set to: getCIGARindels
The run looks good (number of reads read is reported some indels are found, Reports...
