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Comment: C: Identifying mutations from Paired-End Sequencing data
updated 5.4 years ago by 45k • written 11.1 years ago by ▴ 140
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1
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3.4k
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Comment: C: Can'T Find Indels With Samtools (Onyly Get Snps)
updated 5.6 years ago by 45k • written 11.1 years ago by ▴ 140
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2
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1.3k
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Combine several VCF files
vcf bcftools
updated 5.7 years ago by ★ 3.8k • written 5.7 years ago by ▴ 140
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3.9k
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Comment: C: Detecting Structural variants in sequencing data
7.6 years ago by Max Ivon ▴ 140
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3.8k
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Comment: C: Reference and mutant allele of a SNP rsID
7.6 years ago by Max Ivon ▴ 140
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3.8k
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Answer: A: Reference and mutant allele of a SNP rsID
7.6 years ago by Max Ivon ▴ 140
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3.8k
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Comment: C: how to get exact break point in COSMIC fusion gene?
7.7 years ago by Max Ivon ▴ 140
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1.8k
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Comment: C: Multiple biopsy issue in MutSig and GISTIC tools
7.7 years ago by Max Ivon ▴ 140
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1
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1.7k
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Answer: A: Database for Somatic Copy Numbers
7.7 years ago by Max Ivon ▴ 140
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1
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1.3k
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Removing fused transcripts from RNA seq data
RNA-Seq
8.1 years ago by Max Ivon ▴ 140
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0
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3.1k
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Comment: Comment: Bowtie2-Samtools. Too many degenerate bases
updated 2.9 years ago by 45k • written 9.3 years ago by ▴ 140
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0
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1.8k
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Comment: C: How does OMIM select the clinically associated variants (SNPs)?
9.3 years ago by Max Ivon ▴ 140
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6.0k
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Comment: C: samtools mpileup Aborted (Core dumped)
9.3 years ago by Max Ivon ▴ 140
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1
reply
3.1k
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Comment: Comment: Bowtie2-Samtools. Too many degenerate bases
updated 2.8 years ago by 45k • written 9.3 years ago by ▴ 140
0
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1
reply
2.3k
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Comment: Comment: How are the variants called by samtools?
updated 2.8 years ago by 45k • written 9.3 years ago by ▴ 140
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1
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2.4k
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Comment: Comment: NGS hybrid reads
updated 2.8 years ago by 45k • written 9.3 years ago by ▴ 140
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2.4k
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Comment: C: NGS hybrid reads
9.3 years ago by Max Ivon ▴ 140
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1
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2.4k
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Comment: C: NGS hybrid reads
9.3 years ago by Max Ivon ▴ 140
9
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8
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2.4k
views
NGS hybrid reads
next-gen sequencing
updated 2.8 years ago by 45k • written 9.3 years ago by ▴ 140
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0
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3.2k
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Comment: C: Illumina BaseSpace File System
9.5 years ago by Max Ivon ▴ 140
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0
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3.2k
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Comment: C: Illumina BaseSpace File System
9.5 years ago by Max Ivon ▴ 140
0
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9
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3.2k
views
Illumina BaseSpace File System
next-gen-sequencing
updated 2.8 years ago by 45k • written 9.5 years ago by ▴ 140
1
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1
reply
2.2k
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Comment: C: Same locus, more rs IDs
9.6 years ago by Max Ivon ▴ 140
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2.2k
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Answer: Answer: dbSNP SNPHistory file: to what correspond each column?
updated 2.7 years ago by 45k • written 9.7 years ago by ▴ 140
1
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1
reply
1.8k
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Detecting mutations with SNP arrays
snp array
updated 9.8 years ago by 7.3k • written 9.8 years ago by ▴ 140
2
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3
replies
2.8k
views
Distance to reads ends
samtools GATK sequencing SNP
updated 2.6 years ago by 45k • written 9.8 years ago by ▴ 140
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0
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2.8k
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Comment: C: Distance to reads ends
9.8 years ago by Max Ivon ▴ 140
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0
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2.8k
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Comment: Comment: snp microarray data analysis
updated 2.4 years ago by 45k • written 10.0 years ago by ▴ 140
0
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2
replies
2.8k
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snp microarray data analysis
array illumina SNP
updated 2.4 years ago by 45k • written 10.0 years ago by ▴ 140
0
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0
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3.0k
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Comment: Comment: Somatic mutation(indels) in blood sample(autism)
updated 3.3 years ago by 45k • written 10.0 years ago by ▴ 140
0
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1
reply
2.9k
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Comment: C: Clinical utilization of NGS data in cancer research
10.0 years ago by Max Ivon ▴ 140
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0
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2.9k
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Comment: Comment: Clinical utilization of NGS data in cancer research
updated 2.4 years ago by 45k • written 10.0 years ago by ▴ 140
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0
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3.9k
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Comment: Comment: GATK dbSNP for Ensembl
updated 2.4 years ago by 45k • written 10.0 years ago by ▴ 140
6
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6
replies
2.9k
views
Clinical utilization of NGS data in cancer research
ngs allele frequency sequencing cancer
updated 2.4 years ago by 45k • written 10.0 years ago by ▴ 140
2
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1
reply
3.9k
views
Answer: A: GATK dbSNP for Ensembl
10.0 years ago by Max Ivon ▴ 140
0
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1
reply
3.7k
views
Human Exome GC content
gc exome
updated 3.1 years ago by 45k • written 10.3 years ago by ▴ 140
0
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1
reply
2.4k
views
PGM reads 3' end trimming
PGM trimming
updated 3.4 years ago by 45k • written 10.8 years ago by ▴ 140
0
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0
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1.9k
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Ion Torrent PGM reads
PGM
10.8 years ago by Max Ivon ▴ 140
0
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0
replies
2.6k
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Bio-SamTools pileup method
BioPerl PileUp Bio-SamTools
updated 3.4 years ago by 45k • written 10.8 years ago by ▴ 140
2
votes
6
replies
3.4k
views
Can'T Find Indels With Samtools (Onyly Get Snps)
samtools
updated 3.7 years ago by 45k • written 11.2 years ago by ▴ 140
0
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2
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3.4k
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Comment: Comment: Can'T Find Indels With Samtools (Onyly Get Snps)
updated 3.7 years ago by 45k • written 11.1 years ago by ▴ 140
1
vote
3
replies
2.6k
views
Identifying mutations from Paired-End Sequencing data
Mutation sequencing Samtools Paired-end
updated 3.7 years ago by 45k • written 11.1 years ago by ▴ 140
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