3 days ago by
LauferVA
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updated 4 days ago by
Ram
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written 4 days ago by
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updated 4 days ago by
Ram
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written 4 days ago by
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updated 3 days ago by
Ram
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written 4 days ago by
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updated 4 days ago by
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4 days ago by
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4 days ago by
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5 days ago by
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5 days ago by
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updated 5 days ago by
Zhenyu Zhang
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billyK
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updated 7 days ago by
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updated 8 days ago by
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Recent Replies
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I think you will need at least three replicates to be able to do statistics.
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> Asking for bed file is not a suitable option in the current scenario.
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they only provided me the sorted.bam files aligned with hg19. I converted bam into fastq and started variant calling from there. Asking for…
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thanks for the suggestion. how can i obtain the bedfile of my targets (kit is proprietary - can I obtain bed from fasta? if yes how?)
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This may indicate that your R1 and R2 reads were processed in a way that didn't maintain the 1:1 order of matching forward and reverse read…
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Sorry I accidentally hit enter
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how about using the bed file of your targets....
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You should probably be using `MMseqs2`'s `taxonomy` module for this: [https://github.com/soedinglab/MMseqs2#taxonomy][1] .
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Email the developers listed on contact page: https://chlorobox.mpimp-golm.mpg.de/contact.html
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