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4
votes
3
replies
2.4k
views
Find all locations of aligned reads with MQ (Mapping Quality) = 0.
align IGV BAM
updated 21 months ago by ▴ 80 • written 23 months ago by ▴ 20
1
vote
1
reply
787
views
Get VCF-format positions from coding positions
ngs DNA vcf
updated 21 months ago by 45k • written 21 months ago by ▴ 20
0
votes
1
reply
1.3k
views
Comment: Comment: BWA mem align reads with MQ = 0 to only one region (reference genome has two sim
23 months ago by captainlabman ▴ 20
2
votes
3
replies
1.3k
views
BWA mem align reads with MQ = 0 to only one region (reference genome has two similar sequences).
NGS BWA
updated 23 months ago by ★ 1.5k • written 23 months ago by ▴ 20
5
votes
1
reply
1.2k
views
How does tabix work?
annotation tabix ngs vcf
updated 2.0 years ago by 166k • written 2.0 years ago by ▴ 20
1
vote
1
reply
970
views
Find the most similar regions of two dna sequences
sequence DNA
updated 2.3 years ago by 45k • written 2.3 years ago by ▴ 20
0
votes
1
reply
3.6k
views
Comment: Comment: Systematic errors at the end and beginning of reads in NGS panels
2.3 years ago by captainlabman ▴ 20
0
votes
1
reply
3.6k
views
Comment: Comment: Systematic errors at the end and beginning of reads in NGS panels
2.3 years ago by captainlabman ▴ 20
0
votes
1
reply
3.6k
views
Comment: Comment: Systematic errors at the end and beginning of reads in NGS panels
2.3 years ago by captainlabman ▴ 20
0
votes
2
replies
3.6k
views
Comment: Comment: Systematic errors at the end and beginning of reads in NGS panels
2.3 years ago by captainlabman ▴ 20
0
votes
1
reply
3.6k
views
Comment: Comment: Systematic errors at the end and beginning of reads in NGS panels
2.3 years ago by captainlabman ▴ 20
0
votes
2
replies
3.6k
views
Comment: Comment: Systematic errors at the end and beginning of reads in panels
2.3 years ago by captainlabman ▴ 20
0
votes
0
replies
3.6k
views
Comment: Comment: Systematic errors at the end and beginning of reads in panels
2.3 years ago by captainlabman ▴ 20
3
votes
19
replies
3.6k
views
Systematic errors at the end and beginning of reads in NGS panels
sequencing NGS-panels
updated 16 months ago by 45k • written 2.3 years ago by ▴ 20
1
vote
1
reply
635
views
Open human database with RNA sequencing and full genome/exome sequencing (rna-seq + WGS/WES)?
WGS WES rna-seq
updated 3.2 years ago by 2.9k • written 3.2 years ago by ▴ 20
0
votes
0
replies
1.0k
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
4.7 years ago by captainlabman ▴ 20
16 results • Page 1 of 1
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