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Answer: Answer: Making fasta file for clustal
updated 23 months ago by 44k • written 9.5 years ago by ★ 2.7k
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1
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4.4k
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Comment: Comment: Phasing trios for identification of denovo variants
updated 22 months ago by 44k • written 9.5 years ago by ★ 2.7k
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Answer: Answer: Phasing trios for identification of denovo variants
updated 22 months ago by 44k • written 9.5 years ago by ★ 2.7k
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1
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2.3k
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Comment: Comment: Semantic verification of variants
updated 2.4 years ago by 44k • written 9.6 years ago by ★ 2.7k
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3
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Answer: Answer: How to count SNPs, InDels
updated 2.4 years ago by 44k • written 9.6 years ago by ★ 2.7k
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0
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2.4k
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Answer: A: databases of variants
9.6 years ago by Vivek ★ 2.7k
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1
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1.9k
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Answer: A: Is there any tool that gives SNPs list separately in 2 different populations?
9.6 years ago by Vivek ★ 2.7k
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8.3k
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Comment: A: Programatically retrieving CLINVAR records, with the same detail level as it is
9.6 years ago by Vivek ★ 2.7k
1
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0
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2.6k
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Answer: Answer: whre we can get BRCA1 and 2 SNPs data for indian population?
updated 2.5 years ago by 44k • written 9.7 years ago by ★ 2.7k
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3.0k
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Comment: Comment: assign each SNP a strand information
updated 2.5 years ago by 44k • written 9.7 years ago by ★ 2.7k
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1
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3.0k
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Comment: C: assign each SNP a strand information
9.7 years ago by Vivek ★ 2.7k
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1
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3.0k
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Answer: Answer: assign each SNP a strand information
updated 2.5 years ago by 44k • written 9.7 years ago by ★ 2.7k
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0
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4.2k
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Answer: Answer: cuffcompare error: cannot locate input file
updated 2.6 years ago by 44k • written 9.8 years ago by ★ 2.7k
1
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0
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2.5k
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Answer: Answer: Tool to obtain phased genotypes for family quartet?
updated 2.6 years ago by 44k • written 9.8 years ago by ★ 2.7k
0
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1
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3.3k
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Comment: Comment: Reducing sequencing errors in .vcf file
updated 2.6 years ago by 44k • written 9.8 years ago by ★ 2.7k
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1
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3.3k
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Answer: Answer: Reducing sequencing errors in .vcf file
updated 2.6 years ago by 44k • written 9.8 years ago by ★ 2.7k
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0
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3.7k
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Answer: Answer: Pros and cons of using MAF values from earlier as well as from latest release of
updated 3.6 years ago by 44k • written 10.0 years ago by ★ 2.7k
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0
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2.1k
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Comment: Comment: Low quality reads causing false heterozygosity in SNP calling?
updated 2.7 years ago by 44k • written 10.0 years ago by ★ 2.7k
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1
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4.2k
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Comment: C: BLAT does appear anything in the results but blat worked.
10.0 years ago by Vivek ★ 2.7k
0
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1
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4.2k
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Comment: C: BLAT does appear anything in the results but blat worked.
10.0 years ago by Vivek ★ 2.7k
2
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0
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4.6k
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Answer: Answer: How can I learn cluster computing?
updated 2.8 years ago by 44k • written 10.0 years ago by ★ 2.7k
1
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0
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2.6k
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Answer: Answer: Aligning full length primary transcripts to a reference genome
updated 2.8 years ago by 44k • written 10.0 years ago by ★ 2.7k
3
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0
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11k
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Answer: Answer: Select sequences from fastq.gz file
updated 2.8 years ago by 44k • written 10.0 years ago by ★ 2.7k
0
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0
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3.5k
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Comment: C: Determining the accuracy of a "merged" genome assembly
10.0 years ago by Vivek ★ 2.7k
1
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0
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3.0k
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Comment: C: Evolution, not Hadoop, is the Biggest Missing Block in Bioinformatics
10.0 years ago by Vivek ★ 2.7k
4
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1
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10k
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Answer: A: I want to re-open the old debate: python or perl ?
10.0 years ago by Vivek ★ 2.7k
0
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0
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3.6k
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Answer: Answer: what is the best place to find latest phd positions in computational biology esp
updated 2.8 years ago by 44k • written 10.0 years ago by ★ 2.7k
1
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0
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9.5k
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Answer: A: Bioinformatics Mobile App
10.0 years ago by Vivek ★ 2.7k
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0
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5.0k
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Comment: Comment: Discrepancies between 1000 Genomes Phase 1 vs. Phase 3 allele frequencies
updated 2.8 years ago by 44k • written 10.1 years ago by ★ 2.7k
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0
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5.0k
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Comment: Comment: Discrepancies between 1000 Genomes Phase 1 vs. Phase 3 allele frequencies
updated 2.8 years ago by 44k • written 10.1 years ago by ★ 2.7k
1
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1
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5.0k
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Answer: A: Discrepancies between 1000 Genomes Phase 1 vs. Phase 3 allele frequencies
10.1 years ago by Vivek ★ 2.7k
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0
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5.1k
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Comment: C: 1000 Genomes and ESP Populations in Exome Aggregation Consortium Data
10.1 years ago by Vivek ★ 2.7k
0
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1
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5.1k
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Comment: Comment: 1000 Genomes and ESP Populations in Exome Aggregation Consortium Data
updated 2.8 years ago by 44k • written 10.1 years ago by ★ 2.7k
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0
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6.0k
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Comment: Comment: ClinVar download sources
updated 3.7 years ago by 44k • written 10.1 years ago by ★ 2.7k
4
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6
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6.0k
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ClinVar download sources
FTP clinvar Clinical SNP NCBI
updated 3.7 years ago by 44k • written 10.1 years ago by ★ 2.7k
0
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1
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6.0k
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Comment: Comment: ClinVar download sources
updated 3.7 years ago by 44k • written 10.1 years ago by ★ 2.7k
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0
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4.4k
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Answer: A: Calculating genotype likelihood from vcf file which has allele frequency, total
updated 3.7 years ago by 44k • written 10.1 years ago by ★ 2.7k
2
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0
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2.6k
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Comment: C: Exons in Refseq-hg19
10.1 years ago by Vivek ★ 2.7k
0
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0
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7.5k
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Comment: C: align transcripts to genome
10.2 years ago by Vivek ★ 2.7k
0
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1
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11k
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Comment: C: Mpileup On Merged .Bam File
10.2 years ago by Vivek ★ 2.7k
3
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1
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7.5k
views
Answer: Answer: align transcripts to genome
updated 2.9 years ago by 44k • written 10.2 years ago by ★ 2.7k
2
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1
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3.9k
views
Comment: Comment: How to find de novo mutation in trio sequencing data in perl or python script?
updated 2.8 years ago by 44k • written 10.2 years ago by ★ 2.7k
1
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0
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3.6k
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Answer: Answer: Splitting chromosomes in bins of 100kb
updated 2.9 years ago by 44k • written 10.3 years ago by ★ 2.7k
1
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1
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5.4k
views
Comment: Comment: GATK: How to filter variant sites of sample VCF that are not present in a set of
updated 3.1 years ago by 44k • written 10.3 years ago by ★ 2.7k
1
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1
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5.4k
views
Comment: Comment: GATK: How to filter variant sites of sample VCF that are not present in a set of
updated 3.1 years ago by 44k • written 10.3 years ago by ★ 2.7k
0
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1
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5.4k
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Comment: C: GATK: How to filter variant sites of sample VCF that are not present in a set of
10.3 years ago by Vivek ★ 2.7k
1
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2
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5.4k
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Answer: Answer: GATK: How to filter variant sites of sample VCF that are not present in a set of
updated 3.1 years ago by 44k • written 10.3 years ago by ★ 2.7k
0
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0
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4.5k
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Comment: Comment: phasing de novo mutations
updated 2.9 years ago by 44k • written 10.3 years ago by ★ 2.7k
0
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1
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4.5k
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Answer: Answer: phasing de novo mutations
updated 2.9 years ago by 44k • written 10.3 years ago by ★ 2.7k
1
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1
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8.8k
views
Answer: Answer: Retrieve mutation position and ID for a mutation in hgvs format
updated 3.0 years ago by 44k • written 10.4 years ago by ★ 2.7k
232 results • Page 3 of 5
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