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Showing :
answers
4
votes
3
replies
12k
views
Answer:
Answer: How to count SNPs, InDels
updated 22 months ago by
Ram
43k • written 9.0 years ago by
Vivek
★ 2.7k
1
vote
0
replies
2.3k
views
Answer:
A: databases of variants
9.0 years ago by
Vivek
★ 2.7k
0
votes
1
reply
1.8k
views
Answer:
A: Is there any tool that gives SNPs list separately in 2 different populations?
9.1 years ago by
Vivek
★ 2.7k
1
vote
0
replies
2.4k
views
Answer:
Answer: whre we can get BRCA1 and 2 SNPs data for indian population?
updated 23 months ago by
Ram
43k • written 9.1 years ago by
Vivek
★ 2.7k
0
votes
1
reply
2.9k
views
Answer:
Answer: assign each SNP a strand information
updated 23 months ago by
Ram
43k • written 9.2 years ago by
Vivek
★ 2.7k
0
votes
0
replies
4.0k
views
Answer:
Answer: cuffcompare error: cannot locate input file
updated 2.0 years ago by
Ram
43k • written 9.2 years ago by
Vivek
★ 2.7k
1
vote
0
replies
2.4k
views
Answer:
Answer: Tool to obtain phased genotypes for family quartet?
updated 2.0 years ago by
Ram
43k • written 9.2 years ago by
Vivek
★ 2.7k
0
votes
1
reply
3.0k
views
Answer:
Answer: Reducing sequencing errors in .vcf file
updated 2.0 years ago by
Ram
43k • written 9.2 years ago by
Vivek
★ 2.7k
0
votes
0
replies
3.5k
views
Answer:
Answer: Pros and cons of using MAF values from earlier as well as from latest release of
updated 3.1 years ago by
Ram
43k • written 9.4 years ago by
Vivek
★ 2.7k
2
votes
0
replies
4.2k
views
Answer:
Answer: How can I learn cluster computing?
updated 2.2 years ago by
Ram
43k • written 9.4 years ago by
Vivek
★ 2.7k
1
vote
0
replies
2.5k
views
Answer:
Answer: Aligning full length primary transcripts to a reference genome
updated 2.2 years ago by
Ram
43k • written 9.4 years ago by
Vivek
★ 2.7k
3
votes
0
replies
10k
views
Answer:
Answer: Select sequences from fastq.gz file
updated 2.2 years ago by
Ram
43k • written 9.4 years ago by
Vivek
★ 2.7k
4
votes
1
reply
9.7k
views
Answer:
A: I want to re-open the old debate: python or perl ?
9.5 years ago by
Vivek
★ 2.7k
0
votes
0
replies
3.4k
views
Answer:
Answer: what is the best place to find latest phd positions in computational biology esp
updated 2.2 years ago by
Ram
43k • written 9.5 years ago by
Vivek
★ 2.7k
1
vote
0
replies
8.3k
views
Answer:
A: Bioinformatics Mobile App
9.5 years ago by
Vivek
★ 2.7k
1
vote
1
reply
4.8k
views
Answer:
A: Discrepancies between 1000 Genomes Phase 1 vs. Phase 3 allele frequencies
9.5 years ago by
Vivek
★ 2.7k
0
votes
0
replies
4.3k
views
Answer:
A: Calculating genotype likelihood from vcf file which has allele frequency, total
updated 3.1 years ago by
Ram
43k • written 9.6 years ago by
Vivek
★ 2.7k
3
votes
1
reply
7.1k
views
Answer:
Answer: align transcripts to genome
updated 2.3 years ago by
Ram
43k • written 9.6 years ago by
Vivek
★ 2.7k
1
vote
0
replies
3.5k
views
Answer:
Answer: Splitting chromosomes in bins of 100kb
updated 2.4 years ago by
Ram
43k • written 9.7 years ago by
Vivek
★ 2.7k
1
vote
2
replies
5.2k
views
Answer:
Answer: GATK: How to filter variant sites of sample VCF that are not present in a set of
updated 2.5 years ago by
Ram
43k • written 9.7 years ago by
Vivek
★ 2.7k
0
votes
1
reply
4.3k
views
Answer:
Answer: phasing de novo mutations
updated 2.3 years ago by
Ram
43k • written 9.7 years ago by
Vivek
★ 2.7k
1
vote
1
reply
8.5k
views
Answer:
Answer: Retrieve mutation position and ID for a mutation in hgvs format
updated 2.4 years ago by
Ram
43k • written 9.8 years ago by
Vivek
★ 2.7k
1
vote
3
replies
5.2k
views
Answer:
A: Deleted gene appears in RNA-seq analysis?
9.8 years ago by
Vivek
★ 2.7k
1
vote
0
replies
1.8k
views
Answer:
A: Phasing in Trios for unique clinical presentation
9.8 years ago by
Vivek
★ 2.7k
2
votes
1
reply
3.8k
views
Answer:
Answer: while read loop shell command
9.8 years ago by
Vivek
★ 2.7k
0
votes
0
replies
4.8k
views
Answer:
A: How to generate a masked vcf file?
9.9 years ago by
Vivek
★ 2.7k
0
votes
1
reply
103k
views
Answer:
A: How to plot coverage and depth statistics of a bam file
9.9 years ago by
Vivek
★ 2.7k
1
vote
0
replies
2.0k
views
Answer:
A: Looking review paper about; From mapping NGS reads to quantification of gene exp
9.9 years ago by
Vivek
★ 2.7k
0
votes
1
reply
4.5k
views
Answer:
A: How to extract Homozygote variants froma VCF format?
9.9 years ago by
Vivek
★ 2.7k
2
votes
0
replies
3.8k
views
Answer:
Answer: How to safely split a fasta file with concatenated multiple fasta sequences
updated 2.6 years ago by
Ram
43k • written 10.0 years ago by
Vivek
★ 2.7k
1
vote
0
replies
2.6k
views
Answer:
A: Different annotation gtf file in Tophat2 and Cufflink
10.0 years ago by
Vivek
★ 2.7k
0
votes
1
reply
2.9k
views
Answer:
A: What Is The Imprtant Information In The Cufflinks Output Folder
10.1 years ago by
Vivek
★ 2.7k
0
votes
1
reply
5.6k
views
Answer:
A: Program For Flagging Alternative Splicing Events From A Genome Annotation
10.1 years ago by
Vivek
★ 2.7k
2
votes
0
replies
2.5k
views
Answer:
A: Cufflinks On Chromosome 2
10.2 years ago by
Vivek
★ 2.7k
0
votes
0
replies
3.7k
views
Answer:
A: Gene Disease (Cancer) Association
10.3 years ago by
Vivek
★ 2.7k
2
votes
1
reply
5.0k
views
Answer:
A: Why Perl Or Sed Command Not Working
10.3 years ago by
Vivek
★ 2.7k
1
vote
1
reply
11k
views
Answer:
A: Variant Filtration Using Gatk With Ad And Dp
10.4 years ago by
Vivek
★ 2.7k
0
votes
0
replies
3.2k
views
Answer:
A: Variation Count Based On Chromosome
10.4 years ago by
Vivek
★ 2.7k
2
votes
1
reply
5.6k
views
Answer:
A: Error When Convert Mouse Snp137.Txt To .Vcf Format
10.5 years ago by
Vivek
★ 2.7k
0
votes
0
replies
1.9k
views
Answer:
A: Unknown Validation Snps
10.5 years ago by
Vivek
★ 2.7k
1
vote
1
reply
6.8k
views
Answer:
A: Using Paired End And Orphaned Singles For De Novo Assembly
10.6 years ago by
Vivek
★ 2.7k
2
votes
1
reply
3.8k
views
Answer:
A: Resources For Ngs?
10.6 years ago by
Vivek
★ 2.7k
2
votes
1
reply
3.0k
views
Answer:
A: Is Their Any Good Tool For The De Novo Assembly Of Chimeric Reads
10.9 years ago by
Vivek
★ 2.7k
0
votes
1
reply
2.4k
views
Answer:
A: Extract Out The Row Containing Accession Number
10.9 years ago by
Vivek
★ 2.7k
0
votes
0
replies
3.5k
views
Answer:
A: Effect Of Mutation On Codon
11.2 years ago by
Vivek
★ 2.7k
0
votes
1
reply
6.3k
views
Answer:
A: Cnvnator *** Break *** Segmentation Violation
11.4 years ago by
Vivek
★ 2.7k
1
vote
0
replies
2.3k
views
Answer:
A: Variant Calling For Ultra High Coverage Region Of Whole Exome Sequencing Data
11.5 years ago by
Vivek
★ 2.7k
1
vote
1
reply
20k
views
Answer:
A: Get Fasta File With Protein Sequences Given Entrez Gene Ids
11.7 years ago by
Vivek
★ 2.7k
3
votes
1
reply
7.8k
views
Answer:
A: Split Bam Files By Region For Parallel Variant Calling
11.8 years ago by
Vivek
★ 2.7k
0
votes
0
replies
7.3k
views
Answer:
A: Homozygous Ref Calls And No Calls
11.8 years ago by
Vivek
★ 2.7k
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