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Showing :
answers
1
vote
1
reply
4.0k
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Answer:
A: VCF-simplify: a VCF simplification tool.
4.6 years ago by
kirannbishwa01
★ 1.6k
0
votes
0
replies
2.4k
views
Answer:
A: VCF file manipulation for extracting the required information
6.0 years ago by
kirannbishwa01
★ 1.6k
1
vote
0
replies
6.3k
views
Answer:
A: Multisample vcf to table
6.2 years ago by
kirannbishwa01
★ 1.6k
1
vote
0
replies
3.6k
views
Answer:
A: VCF simplify INFO
6.2 years ago by
kirannbishwa01
★ 1.6k
0
votes
0
replies
2.0k
views
Answer:
A: Is this GT a mistake?
6.3 years ago by
kirannbishwa01
★ 1.6k
1
vote
1
reply
2.0k
views
Answer:
A: Is this GT a mistake?
6.3 years ago by
kirannbishwa01
★ 1.6k
1
vote
1
reply
1.9k
views
Answer:
A: detecting allele specific expression of a gene at a specific locus without havin
6.6 years ago by
kirannbishwa01
★ 1.6k
4
votes
0
replies
6.2k
views
Answer:
A: Bam to fastq conversion is giving error?
6.9 years ago by
kirannbishwa01
★ 1.6k
4
votes
0
replies
4.2k
views
Answer:
Answer: GATK method for filtering vcf lines using GT values at all or multisample level.
2.2 years ago by
kirannbishwa01
★ 1.6k
0
votes
0
replies
1.8k
views
Answer:
A: How to select specific values (features and attributes) from gtf/gff file and co
7.0 years ago by
kirannbishwa01
★ 1.6k
2
votes
0
replies
3.1k
views
Answer:
A: Which software can be used to extend the partially phased vcf from several diffe
7.1 years ago by
kirannbishwa01
★ 1.6k
1
vote
0
replies
3.2k
views
Answer:
A: variant calling after mapping via bwa mem
7.3 years ago by
kirannbishwa01
★ 1.6k
0
votes
0
replies
3.4k
views
Answer:
A: How to call genotype bases for all the samples?
7.3 years ago by
kirannbishwa01
★ 1.6k
47
votes
2
replies
103k
views
Answer:
A: How to plot coverage and depth statistics of a bam file
7.5 years ago by
kirannbishwa01
★ 1.6k
2
votes
0
replies
15k
views
Answer:
A: How to select aligned reads below certain mapping Quality (from BWA)?
7.6 years ago by
kirannbishwa01
★ 1.6k
24
votes
0
replies
39k
views
Answer:
A: Bedtools Genomecoveragebed Usage : How To Create A Genome File?
7.6 years ago by
kirannbishwa01
★ 1.6k
2
votes
0
replies
15k
views
Answer:
A: How to select aligned reads below certain mapping Quality (from BWA)?
7.6 years ago by
kirannbishwa01
★ 1.6k
1
vote
1
reply
2.4k
views
Answer:
A: Biology side of bioinformatics
7.7 years ago by
kirannbishwa01
★ 1.6k
0
votes
2
replies
5.9k
views
Answer:
A: Pysam is giving - ValueError: reference_id -1 out of range 0<=tid<65334. Any su
7.9 years ago by
kirannbishwa01
★ 1.6k
0
votes
1
reply
3.1k
views
Answer:
A: Adapter trimming in basespace
7.9 years ago by
kirannbishwa01
★ 1.6k
1
vote
0
replies
11k
views
Answer:
A: Why GATK and bcftools SNP calling different?
8.1 years ago by
kirannbishwa01
★ 1.6k
2
votes
2
replies
11k
views
Answer:
A: Why GATK and bcftools SNP calling different?
8.1 years ago by
kirannbishwa01
★ 1.6k
6
votes
1
reply
11k
views
Answer:
A: Why GATK and bcftools SNP calling different?
8.1 years ago by
kirannbishwa01
★ 1.6k
0
votes
0
replies
4.1k
views
Answer:
A: How can I best use -c in bwa mem for alignment and to find polymorphisms?
8.2 years ago by
kirannbishwa01
★ 1.6k
0
votes
1
reply
5.2k
views
Answer:
A: Viewing the tophat output (mapped.bam and junctions) along with genome coordinat
8.8 years ago by
kirannbishwa01
★ 1.6k
0
votes
1
reply
5.2k
views
Answer:
A: Viewing the tophat output (mapped.bam and junctions) along with genome coordinat
8.8 years ago by
kirannbishwa01
★ 1.6k
0
votes
0
replies
2.0k
views
Answer:
Answer: Alignment of genomic resequenced data to reference genome
updated 2.0 years ago by
Ram
43k • written 9.2 years ago by
kirannbishwa01
★ 1.6k
27 results • Page
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