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Comment: C: Adding bam file (Any file) as URL
5.7 years ago by rse ▴ 100
0
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0
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2.4k
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Comment: C: Adding bam file (Any file) as URL
5.7 years ago by rse ▴ 100
0
votes
0
replies
2.4k
views
Comment: C: Adding bam file (Any file) as URL
5.7 years ago by rse ▴ 100
10
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11
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2.4k
views
7 follow
Adding bam file (Any file) as URL
next-gen sequencing
updated 5.7 years ago by ★ 3.5k • written 5.7 years ago by ▴ 100
0
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2
replies
2.4k
views
Comment: C: Adding bam file (Any file) as URL
5.7 years ago by rse ▴ 100
0
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1
reply
2.4k
views
Comment: A: Adding bam file (Any file) as URL
5.7 years ago by rse ▴ 100
3
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4
replies
1.2k
views
Upload data files on web server
SNP
updated 5.9 years ago by 20 • written 6.1 years ago by ▴ 100
0
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0
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1.4k
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Answer: A: What to do to identify rare variatns from vcf files resulted from UnifiedGenotyp
6.0 years ago by rse ▴ 100
0
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1
reply
924
views
Replace read group
genome sequencing
6.0 years ago by rse ▴ 100
0
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0
replies
3.7k
views
Comment: C: What is Read Group platform??
6.0 years ago by rse ▴ 100
1
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1
reply
3.7k
views
Comment: A: What is Read Group platform??
6.1 years ago by rse ▴ 100
0
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0
replies
5.1k
views
Comment: C: Does vcf-consensus support indels?
6.1 years ago by rse ▴ 100
0
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0
replies
31k
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Comment: C: GT and GL fields in VCF file
6.1 years ago by rse ▴ 100
0
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0
replies
4.4k
views
Comment: C: Fasta sequence from Bam file
6.1 years ago by rse ▴ 100
0
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1
reply
4.4k
views
Comment: C: Fasta sequence from Bam file
6.1 years ago by rse ▴ 100
0
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1
reply
4.4k
views
Comment: C: Fasta sequence from Bam file
6.1 years ago by rse ▴ 100
0
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1
reply
4.4k
views
Comment: C: Fasta sequence from Bam file
6.1 years ago by rse ▴ 100
0
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1
reply
4.4k
views
Comment: A: Fasta sequence from Bam file
6.1 years ago by rse ▴ 100
2
votes
10
replies
4.4k
views
Fasta sequence from Bam file
genome next-gen sequencing
6.1 years ago by rse ▴ 100
0
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0
replies
8.0k
views
Comment: A: Polygenic Risk Score PLINK
6.2 years ago by rse ▴ 100
0
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5
replies
3.3k
views
IGV Visualization Insert Size
next-gen sequencing alignment
updated 6.3 years ago by 20 • written 6.3 years ago by ▴ 100
0
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0
replies
1.1k
views
Answer: A: No coverage or very low coverage in the Complete Genomics data
6.3 years ago by rse ▴ 100
0
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3
replies
1.1k
views
No coverage or very low coverage in the Complete Genomics data
next-gen sequencing
6.3 years ago by rse ▴ 100
1
vote
4
replies
1.4k
views
Visualization software for large variations
alignment next-gen sequencing
6.3 years ago by rse ▴ 100
0
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0
replies
1.4k
views
Answer: A: Visualization software for large variations
6.3 years ago by rse ▴ 100
0
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0
replies
1.1k
views
Comment: C: No coverage or very low coverage in the Complete Genomics data
6.3 years ago by rse ▴ 100
0
votes
1
reply
2.0k
views
(Closed) IGV Visualization Insert Size
alignment next-gen sequencing
updated 6.3 years ago by 87k • written 6.4 years ago by ▴ 100
0
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1
reply
3.3k
views
Comment: C: IGV Visualization Insert Size
6.3 years ago by rse ▴ 100
0
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0
replies
1.4k
views
Comment: A: Visualization software for large variations
6.3 years ago by rse ▴ 100
1
vote
4
replies
2.4k
views
Loss of heterozygosity analysis from SNV files
next-gen sequencing
updated 6.8 years ago by ★ 1.4k • written 7.0 years ago by ▴ 100
0
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0
replies
2.4k
views
Answer: A: Loss of heterozygosity analysis from SNV files
7.0 years ago by rse ▴ 100
0
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0
replies
6.0k
views
Comment: C: Loss Of Heterozygosity Calls On Snp Annotated File
7.0 years ago by rse ▴ 100
0
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0
replies
2.7k
views
Comment: C: CNV / SV Filtration
7.0 years ago by rse ▴ 100
0
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0
replies
2.7k
views
Comment: C: CNV / SV Filtration
7.0 years ago by rse ▴ 100
0
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1
reply
2.7k
views
Comment: C: CNV / SV Filtration
7.0 years ago by rse ▴ 100
0
votes
0
replies
2.4k
views
Comment: Comment: SNVer error: chrome not found in Reference
7.7 years ago by rse ▴ 100
15
votes
11
replies
4.2k
views
8 follow
Learn to develop bioinformatics tools
software-development
updated 10 months ago by 43k • written 7.8 years ago by ▴ 100
0
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0
replies
4.2k
views
Answer: A: Learn to develop bioinformatics tools
7.7 years ago by rse ▴ 100
0
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0
replies
4.2k
views
Comment: C: Learn to develop bioinformatics tools
7.7 years ago by rse ▴ 100
0
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0
replies
3.8k
views
Comment: C: Retrieving gene names from list of mRNA accession IDs
7.8 years ago by rse ▴ 100
4
votes
4
replies
3.8k
views
Retrieving gene names from list of mRNA accession IDs
next-gen
7.9 years ago by rse ▴ 100
0
votes
0
replies
9.9k
views
Comment: C: gistic for whole genome sequencing copy number analysis
7.9 years ago by rse ▴ 100
0
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0
replies
4.8k
views
Comment: A: Why does GISTIC require a markers file?
7.9 years ago by rse ▴ 100
0
votes
0
replies
3.4k
views
Comment: C: Cnv Analysis After Segmentations
7.9 years ago by rse ▴ 100
0
votes
0
replies
7.9k
views
Comment: C: GISTIC 2.0 Segment CN
7.9 years ago by rse ▴ 100
0
votes
1
reply
9.9k
views
Comment: C: gistic for whole genome sequencing copy number analysis
7.9 years ago by rse ▴ 100
1
vote
0
replies
1.8k
views
Answer: A: Depth of coverage
7.9 years ago by rse ▴ 100
0
votes
0
replies
2.6k
views
Answer: A: visualizing software for alignment
7.9 years ago by rse ▴ 100
0
votes
0
replies
15k
views
Comment: C: Extracting Individual Allele Frequencies From A Vcf File
7.9 years ago by rse ▴ 100
0
votes
0
replies
1.4k
views
DNACopy package for genome segmentation
next-gen
7.9 years ago by rse ▴ 100
117 results • Page 2 of 3
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