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Comment: C: Adding bam file (Any file) as URL
6.6 years ago by rse ▴ 100
0
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0
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3.0k
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Comment: C: Adding bam file (Any file) as URL
6.6 years ago by rse ▴ 100
0
votes
0
replies
3.0k
views
Comment: C: Adding bam file (Any file) as URL
6.6 years ago by rse ▴ 100
10
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11
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3.0k
views
7 follow
Adding bam file (Any file) as URL
next-gen sequencing
updated 6.6 years ago by ★ 3.5k • written 6.6 years ago by ▴ 100
0
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2
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3.0k
views
Comment: C: Adding bam file (Any file) as URL
6.6 years ago by rse ▴ 100
0
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1
reply
3.0k
views
Comment: A: Adding bam file (Any file) as URL
6.6 years ago by rse ▴ 100
3
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4
replies
1.3k
views
Upload data files on web server
SNP
updated 6.9 years ago by 20 • written 7.1 years ago by ▴ 100
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0
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1.7k
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Answer: A: What to do to identify rare variatns from vcf files resulted from UnifiedGenotyp
7.0 years ago by rse ▴ 100
0
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1
reply
1.0k
views
Replace read group
genome sequencing
7.0 years ago by rse ▴ 100
0
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0
replies
4.3k
views
Comment: C: What is Read Group platform??
7.0 years ago by rse ▴ 100
1
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1
reply
4.3k
views
Comment: A: What is Read Group platform??
7.0 years ago by rse ▴ 100
0
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0
replies
5.8k
views
Comment: C: Does vcf-consensus support indels?
7.1 years ago by rse ▴ 100
0
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0
replies
34k
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Comment: C: GT and GL fields in VCF file
7.1 years ago by rse ▴ 100
0
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0
replies
4.9k
views
Comment: C: Fasta sequence from Bam file
7.1 years ago by rse ▴ 100
0
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1
reply
4.9k
views
Comment: C: Fasta sequence from Bam file
7.1 years ago by rse ▴ 100
0
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1
reply
4.9k
views
Comment: C: Fasta sequence from Bam file
7.1 years ago by rse ▴ 100
0
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1
reply
4.9k
views
Comment: C: Fasta sequence from Bam file
7.1 years ago by rse ▴ 100
0
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1
reply
4.9k
views
Comment: A: Fasta sequence from Bam file
7.1 years ago by rse ▴ 100
2
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10
replies
4.9k
views
Fasta sequence from Bam file
genome next-gen sequencing
7.1 years ago by rse ▴ 100
0
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0
replies
8.4k
views
Comment: A: Polygenic Risk Score PLINK
7.2 years ago by rse ▴ 100
0
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5
replies
4.0k
views
IGV Visualization Insert Size
next-gen sequencing alignment
updated 7.3 years ago by 20 • written 7.3 years ago by ▴ 100
0
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0
replies
1.3k
views
Answer: A: No coverage or very low coverage in the Complete Genomics data
7.3 years ago by rse ▴ 100
0
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3
replies
1.3k
views
No coverage or very low coverage in the Complete Genomics data
next-gen sequencing
7.3 years ago by rse ▴ 100
1
vote
4
replies
1.6k
views
Visualization software for large variations
alignment next-gen sequencing
7.3 years ago by rse ▴ 100
0
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0
replies
1.6k
views
Answer: A: Visualization software for large variations
7.3 years ago by rse ▴ 100
0
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0
replies
1.3k
views
Comment: C: No coverage or very low coverage in the Complete Genomics data
7.3 years ago by rse ▴ 100
0
votes
1
reply
2.2k
views
(Closed) IGV Visualization Insert Size
alignment next-gen sequencing
updated 7.3 years ago by 89k • written 7.4 years ago by ▴ 100
0
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1
reply
4.0k
views
Comment: C: IGV Visualization Insert Size
7.3 years ago by rse ▴ 100
0
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0
replies
1.6k
views
Comment: A: Visualization software for large variations
7.3 years ago by rse ▴ 100
1
vote
4
replies
2.7k
views
Loss of heterozygosity analysis from SNV files
next-gen sequencing
updated 7.8 years ago by ★ 1.4k • written 8.0 years ago by ▴ 100
0
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0
replies
2.7k
views
Answer: A: Loss of heterozygosity analysis from SNV files
8.0 years ago by rse ▴ 100
0
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0
replies
7.0k
views
Comment: C: Loss Of Heterozygosity Calls On Snp Annotated File
8.0 years ago by rse ▴ 100
0
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0
replies
3.2k
views
Comment: C: CNV / SV Filtration
8.0 years ago by rse ▴ 100
0
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0
replies
3.2k
views
Comment: C: CNV / SV Filtration
8.0 years ago by rse ▴ 100
0
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1
reply
3.2k
views
Comment: C: CNV / SV Filtration
8.0 years ago by rse ▴ 100
0
votes
0
replies
2.7k
views
Comment: Comment: SNVer error: chrome not found in Reference
8.7 years ago by rse ▴ 100
0
votes
0
replies
4.9k
views
Answer: A: Learn to develop bioinformatics tools
8.7 years ago by rse ▴ 100
15
votes
11
replies
4.9k
views
8 follow
Learn to develop bioinformatics tools
software-development
updated 22 months ago by 45k • written 8.8 years ago by ▴ 100
0
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0
replies
4.9k
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Comment: C: Learn to develop bioinformatics tools
8.7 years ago by rse ▴ 100
0
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0
replies
4.1k
views
Comment: C: Retrieving gene names from list of mRNA accession IDs
8.8 years ago by rse ▴ 100
4
votes
4
replies
4.1k
views
Retrieving gene names from list of mRNA accession IDs
next-gen
8.8 years ago by rse ▴ 100
0
votes
0
replies
11k
views
Comment: C: gistic for whole genome sequencing copy number analysis
8.9 years ago by rse ▴ 100
0
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0
replies
5.2k
views
Comment: A: Why does GISTIC require a markers file?
8.9 years ago by rse ▴ 100
0
votes
0
replies
3.8k
views
Comment: C: Cnv Analysis After Segmentations
8.9 years ago by rse ▴ 100
0
votes
0
replies
8.6k
views
Comment: C: GISTIC 2.0 Segment CN
8.9 years ago by rse ▴ 100
0
votes
1
reply
11k
views
Comment: C: gistic for whole genome sequencing copy number analysis
8.9 years ago by rse ▴ 100
1
vote
0
replies
2.0k
views
Answer: A: Depth of coverage
8.9 years ago by rse ▴ 100
0
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0
replies
3.0k
views
Answer: A: visualizing software for alignment
8.9 years ago by rse ▴ 100
0
votes
0
replies
15k
views
Comment: C: Extracting Individual Allele Frequencies From A Vcf File
8.9 years ago by rse ▴ 100
0
votes
0
replies
1.5k
views
DNACopy package for genome segmentation
next-gen
8.9 years ago by rse ▴ 100
117 results • Page 2 of 3
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