8
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2
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548
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2
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written 7 months ago by
finswimmer ♦ 7.0k
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26 minutes ago by
Biostar ♦♦ 20
2
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2
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4.0k
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2
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Sukhdeep Singh ♦ 9.5k
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1 hour ago by
qliu • 0
4
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0
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65
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0
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juansantiago.medina • 40
• updated
1 hour ago by
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2
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1
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68
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1
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Biojl • 1.6k
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2 hours ago by
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2
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0
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Tutorial:
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1
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1
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116
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1
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zhou_1228 • 0
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3 hours ago by
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2
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93
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8 follow
2
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4 hours ago by
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385
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Istvan Albert ♦♦ 78k
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6 hours ago by
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0
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0
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141
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896
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sharon.e.hook • 0
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7 hours ago by
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1
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0
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58
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Molly_K • 40
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devidjohn47 • 0
0
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0
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36
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0
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1
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49
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1
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filippodellanno39 • 0
• updated
8 hours ago by
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3
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10 hours ago by
Kevin Blighe ♦ 32k
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Recent Replies
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C: How to split BAM files by samples from PacBio by
jharting • 0
You should also be using the option `--same`, assuming your barcodes are the same on both ends of...
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C: How can keep the change in my fastq file when i use grep and sed to edit it? by
h.mon ♦ 21k
Out of curiosity: **why** do you want to add "ILLUMINA" to every header?
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C: help identifying bioinformatics operations tools by
genomax ♦ 58k
Basically you are looking for a NGS Laboratory Information Management system (LIMS). Open source/...
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qliu • 0
Have you considered clean-up or size selection before PCR? Even though the software tools can hel...
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C: help identifying bioinformatics operations tools by
RamRS ♦ 19k
Moved post to forum.
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RamRS ♦ 19k
Do not add an answer unless you're answering the top level question; Use the `Add Comment` or `Ad...
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C: How can keep the change in my fastq file when i use grep and sed to edit it? by
RamRS ♦ 19k
Agreed. Don't use the `-i` switch unless you're really sure what the sed does *and* you're sure y...
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mugambigenes90 • 0
what's the unix command to open fasta file?
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Dear Biojl, currently there is no way to directly get the cds sequences from all the proteins in...
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I think you are having trouble with a few concepts here. - there is no easy transforming of gen...
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Install and use [GNU Parallel](https://www.gnu.org/software/parallel/). Then use the following m...
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So I did some looking at my bam file headers and noticed that some of the samples were ran with d...
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