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captainlabman
captainlabman
Reputation:
20 (New)
Joined:
5.6 years ago
Last seen:
2.5 years ago
Location:
Russia
Latest posts by user
1 vote
1 reply
1.0K views
Get VCF-format positions from coding positions
ngs dna vcf
updated by Ram 4.5K • | written by captainlabman 2
0 votes
1 reply
0 views
Comment: Comment: BWA mem align reads with MQ = 0 to only one region (reference genome has two sim
written by captainlabman 2
0 votes
3 replies
1.5K views
BWA mem align reads with MQ = 0 to only one region (reference genome has two similar sequences).
ngs bwa
updated by Raony Guimarães 153 • | written by captainlabman 2
0 votes
3 replies
3.1K views
Find all locations of aligned reads with MQ (Mapping Quality) = 0.
align igv bam
updated by clealk 8 • | written by captainlabman 2
1 vote
1 reply
1.6K views
How does tabix work?
annotation tabix ngs vcf
updated by Pierre Lindenbaum 17K • | written by captainlabman 2
0 votes
1 reply
1.1K views
Find the most similar regions of two dna sequences
sequence dna
updated by Ram 4.5K • | written by captainlabman 2
0 votes
1 reply
0 views
Comment: Comment: Systematic errors at the end and beginning of reads in NGS panels
written by captainlabman 2
0 votes
1 reply
0 views
Comment: Comment: Systematic errors at the end and beginning of reads in NGS panels
written by captainlabman 2
0 votes
1 reply
0 views
Comment: Comment: Systematic errors at the end and beginning of reads in NGS panels
written by captainlabman 2
0 votes
2 replies
0 views
Comment: Comment: Systematic errors at the end and beginning of reads in NGS panels
written by captainlabman 2
0 votes
1 reply
0 views
Comment: Comment: Systematic errors at the end and beginning of reads in NGS panels
written by captainlabman 2
0 votes
2 replies
0 views
Comment: Comment: Systematic errors at the end and beginning of reads in panels
written by captainlabman 2
0 votes
0 replies
0 views
Comment: Comment: Systematic errors at the end and beginning of reads in panels
written by captainlabman 2
0 votes
19 replies
4.1K views
Systematic errors at the end and beginning of reads in NGS panels
sequencing ngs-panels
updated by Ram 4.5K • | written by captainlabman 2
0 votes
1 reply
768 views
Open human database with RNA sequencing and full genome/exome sequencing (rna-seq + WGS/WES)?
wgs wes rna-seq
updated by 4galaxy77 288 • | written by captainlabman 2
0 votes
0 replies
1.1K views
Getting a list of variants (SNPs/mutations) using the Ensembl IDs (ENST) or NCBI IDs (NM) using Python 3. Or another way to get it using Python 3.
snp
written by captainlabman 2
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TODO: Awards