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4
votes
3
replies
587
views
Find all locations of aligned reads with MQ (Mapping Quality) = 0.
align IGV BAM
updated 3 months ago by ▴ 50 • written 6 months ago by ▴ 20
1
vote
1
reply
270
views
Get VCF-format positions from coding positions
ngs DNA vcf
updated 3 months ago by 44k • written 3 months ago by ▴ 20
2
votes
3
replies
597
views
BWA mem align reads with MQ = 0 to only one region (reference genome has two similar sequences).
NGS BWA
updated 6 months ago by ★ 1.4k • written 6 months ago by ▴ 20
5
votes
1
reply
477
views
How does tabix work?
annotation tabix ngs vcf
updated 6 months ago by 162k • written 6 months ago by ▴ 20
1
vote
1
reply
461
views
Find the most similar regions of two dna sequences
sequence DNA
updated 10 months ago by 44k • written 10 months ago by ▴ 20
3
votes
19
replies
1.6k
views
Systematic errors at the end and beginning of reads in NGS panels
NGS error panels sequencing
updated 10 months ago by 10k • written 10 months ago by ▴ 20
1
vote
1
reply
397
views
Open human database with RNA sequencing and full genome/exome sequencing (rna-seq + WGS/WES)?
WGS WES rna-seq
updated 21 months ago by 2.8k • written 21 months ago by ▴ 20
0
votes
0
replies
829
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
3.2 years ago by captainlabman ▴ 20
8 results • Page 1 of 1
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