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0
votes
0
replies
992
views
Comment: Comment: VarDict in paired end mode with GATK preprocessing
2.7 years ago by kulvait ▴ 290
0
votes
2
replies
992
views
VarDict in paired end mode with GATK preprocessing
vardict exomeseq variant discovery
2.7 years ago by kulvait ▴ 290
20
votes
7
replies
14k
views
Determine sex from vcf file (or sequencing data)
variant genotyping vcf
updated 3.5 years ago by ▴ 130 • written 9.4 years ago by ▴ 290
3
votes
8
replies
3.0k
views
For bam and mutation signature I need coverage and number of observations
next-gen vcf bam
updated 8.1 years ago by 21k • written 8.9 years ago by ▴ 290
3
votes
2
replies
1.7k
views
Strip primer sequences from sequencing reads
DNA-seq amplicon-seq BAM
updated 8.1 years ago by ▴ 640 • written 8.1 years ago by ▴ 290
0
votes
1
reply
2.6k
views
Comment: C: Finding sample swaps using VCF files
8.1 years ago by kulvait ▴ 290
2
votes
4
replies
2.6k
views
Finding sample swaps using VCF files
dna-seq amplicon-seq vcf
8.1 years ago by kulvait ▴ 290
0
votes
0
replies
2.2k
views
Comment: C: Weird alignments in amplicon sequencing
8.9 years ago by kulvait ▴ 290
1
vote
0
replies
3.0k
views
Comment: C: For bam and mutation signature I need coverage and number of observations
8.9 years ago by kulvait ▴ 290
0
votes
1
reply
3.0k
views
Comment: C: For bam and mutation signature I need coverage and number of observations
8.9 years ago by kulvait ▴ 290
0
votes
2
replies
3.0k
views
Comment: A: For bam and mutation signature I need coverage and number of observations
8.9 years ago by kulvait ▴ 290
0
votes
0
replies
3.1k
views
Comment: C: IndelRealigner and RealignerTargetCreator for amplicon sequencing
8.9 years ago by kulvait ▴ 290
0
votes
0
replies
3.1k
views
Comment: C: IndelRealigner and RealignerTargetCreator for amplicon sequencing
8.9 years ago by kulvait ▴ 290
3
votes
4
replies
3.1k
views
IndelRealigner and RealignerTargetCreator for amplicon sequencing
amplicon-seq NGS indel
updated 8.9 years ago by 48k • written 8.9 years ago by ▴ 290
0
votes
2
replies
2.2k
views
Weird alignments in amplicon sequencing
amplicon-seq sequencing myeloid
8.9 years ago by kulvait ▴ 290
0
votes
0
replies
6.8k
views
Comment: C: samtools v1.3: AD, ADF and ADR fields
9.3 years ago by kulvait ▴ 290
2
votes
1
reply
2.7k
views
Answer: A: Does the order of the RMA algorithm make a difference in results?
9.3 years ago by kulvait ▴ 290
0
votes
1
reply
2.7k
views
Comment: C: Genome assembly process
9.4 years ago by kulvait ▴ 290
8
votes
0
replies
14k
views
Answer: A: Determine sex from vcf file (or sequencing data)
9.4 years ago by kulvait ▴ 290
3
votes
0
replies
14k
views
Answer: A: Determine sex from vcf file (or sequencing data)
9.4 years ago by kulvait ▴ 290
1
vote
9
replies
2.7k
views
Genome assembly process
DNA
updated 9.4 years ago by 33k • written 9.4 years ago by ▴ 290
0
votes
0
replies
2.7k
views
Comment: C: Genome assembly process
9.4 years ago by kulvait ▴ 290
0
votes
0
replies
14k
views
Comment: C: Determine sex from vcf file (or sequencing data)
9.4 years ago by kulvait ▴ 290
0
votes
0
replies
5.1k
views
Comment: C: Remove duplicates from exome sequencing data
9.4 years ago by kulvait ▴ 290
2
votes
1
reply
5.1k
views
Answer: A: Remove duplicates from exome sequencing data
9.4 years ago by kulvait ▴ 290
9
votes
9
replies
5.1k
views
Remove duplicates from exome sequencing data
variants sequencing exome-seq
9.4 years ago by kulvait ▴ 290
1
vote
1
reply
5.1k
views
Comment: C: Remove duplicates from exome sequencing data
9.4 years ago by kulvait ▴ 290
9
votes
9
replies
3.0k
views
How to parse info field in Excel
sequencing
updated 9.5 years ago by ★ 3.2k • written 9.5 years ago by ▴ 290
0
votes
1
reply
3.0k
views
Comment: C: How to parse info field in Excel
9.5 years ago by kulvait ▴ 290
0
votes
1
reply
3.0k
views
Comment: C: How to parse info field in Excel
9.5 years ago by kulvait ▴ 290
0
votes
0
replies
1.8k
views
SnpEff protein_protein_contact annotation
SNP ngs
9.5 years ago by kulvait ▴ 290
0
votes
0
replies
9.9k
views
Answer: A: Variant caller for low frequency variants
9.5 years ago by kulvait ▴ 290
1
vote
6
replies
7.0k
views
Filtering bam files generated by bwa mem
next-gen sequencing SNP
9.5 years ago by kulvait ▴ 290
0
votes
0
replies
7.0k
views
Answer: A: Filtering bam files generated by bwa mem
9.5 years ago by kulvait ▴ 290
9
votes
7
replies
9.9k
views
Variant caller for low frequency variants
NGS
9.5 years ago by kulvait ▴ 290
0
votes
0
replies
7.0k
views
Comment: C: Filtering bam files generated by bwa mem
9.5 years ago by kulvait ▴ 290
0
votes
0
replies
10k
views
Answer: Answer: bcftools: invalid option -- b was showed error
updated 3.6 years ago by 45k • written 9.5 years ago by ▴ 290
0
votes
1
reply
9.9k
views
Comment: A: Variant caller for low frequency variants
9.5 years ago by kulvait ▴ 290
1
vote
0
replies
4.1k
views
Answer: A: How Could I Handle Bed Files In Java?
updated 10.4 years ago by 5.1k • written 10.4 years ago by ▴ 290
2
votes
1
reply
1.8k
views
Dealing with sequencing data annotations
sequencing annotation
updated 3.2 years ago by 45k • written 10.4 years ago by ▴ 290
40 results • Page 1 of 1
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