Profile Posts Awards
Show
all questions tools blogs news tutorials forum answers comments
Showing : comments
2
votes
1
reply
4.7k
views
Comment: C: CNV analysis from exome data (heterozygous vs homozygous)
updated 4.3 years ago by 43k • written 9.9 years ago by ★ 1.1k
1
vote
1
reply
3.3k
views
Comment: C: Variant Callers for deep sequencing
updated 4.3 years ago by 43k • written 9.9 years ago by ★ 1.1k
0
votes
1
reply
3.6k
views
Comment: C: Getting Population Specific Allele Frequency For Illumina Genotyping Data
updated 4.3 years ago by 43k • written 10.0 years ago by ★ 1.1k
0
votes
0
replies
5.2k
views
Comment: C: More than one transcript per protein in Uniprot
updated 4.3 years ago by 43k • written 10.0 years ago by ★ 1.1k
0
votes
1
reply
2.3k
views
Comment: C: GWAS using 1kg or other database as "controls"?
updated 4.3 years ago by 43k • written 10.0 years ago by ★ 1.1k
1
vote
1
reply
2.5k
views
Comment: C: PLINK 1.90 alpha
updated 4.3 years ago by 43k • written 10.0 years ago by ★ 1.1k
1
vote
1
reply
2.9k
views
Comment: C: Ideas or advise for data visualization that shows genotype and phenotpye relatio
updated 4.3 years ago by 43k • written 10.0 years ago by ★ 1.1k
3
votes
1
reply
2.7k
views
Comment: C: What's the correct way to withdraw a published database/server ?
updated 4.3 years ago by 43k • written 10.0 years ago by ★ 1.1k
1
vote
1
reply
3.8k
views
Comment: Comment: For the general public seeking advice from this community
updated 19 months ago by 43k • written 8.6 years ago by ★ 1.1k
0
votes
1
reply
3.6k
views
Comment: C: Getting Population Specific Allele Frequency For Illumina Genotyping Data
9.1 years ago by Katie D'Aco ★ 1.1k
1
vote
1
reply
6.0k
views
Comment: Comment: Mission Impossible: you have 1 minute to analyze the Ebola Genome
updated 2.2 years ago by 43k • written 9.5 years ago by ★ 1.1k
1
vote
1
reply
8.4k
views
Comment: C: Back-filling missing genotypes in merged VCF
9.5 years ago by Katie D'Aco ★ 1.1k
0
votes
1
reply
3.5k
views
Comment: Comment: What bioinformatics tools/software do not get enough recognition?
updated 2.2 years ago by 43k • written 9.5 years ago by ★ 1.1k
1
vote
0
replies
3.4k
views
Comment: C: Public Disease Exomes (VCF)
9.5 years ago by Katie D'Aco ★ 1.1k
0
votes
0
replies
2.8k
views
Comment: Comment: combining sequencing variants
updated 2.3 years ago by 43k • written 9.6 years ago by ★ 1.1k
1
vote
1
reply
4.6k
views
Comment: C: Template-specific primers design
9.7 years ago by Katie D'Aco ★ 1.1k
0
votes
1
reply
4.6k
views
Comment: C: Template-specific primers design
9.7 years ago by Katie D'Aco ★ 1.1k
0
votes
1
reply
7.2k
views
Comment: C: Pre-computed list of genes in LD with a SNP with r2 from 1000Genomes / hg19
9.7 years ago by Katie D'Aco ★ 1.1k
0
votes
1
reply
2.0k
views
Comment: Comment: WES data - first exon
updated 2.4 years ago by 43k • written 9.7 years ago by ★ 1.1k
0
votes
0
replies
7.1k
views
Comment: C: Immune repertoire sequencing community
9.7 years ago by Katie D'Aco ★ 1.1k
0
votes
1
reply
7.1k
views
Comment: C: Immune repertoire sequencing community
9.7 years ago by Katie D'Aco ★ 1.1k
0
votes
1
reply
3.9k
views
Comment: C: Burden test interpretation
9.7 years ago by Katie D'Aco ★ 1.1k
0
votes
1
reply
3.9k
views
Comment: C: Burden test interpretation
9.7 years ago by Katie D'Aco ★ 1.1k
0
votes
1
reply
2.5k
views
Comment: C: Selection of family samples for exome sequencing study
9.7 years ago by Katie D'Aco ★ 1.1k
1
vote
0
replies
2.5k
views
Comment: C: Question about homozygous concept in a paper sentence
9.7 years ago by Katie D'Aco ★ 1.1k
0
votes
2
replies
3.7k
views
Comment: C: Custom database for genomic data
9.8 years ago by Katie D'Aco ★ 1.1k
0
votes
1
reply
1.5k
views
Comment: C: pVAAST Complex Disease
9.8 years ago by Katie D'Aco ★ 1.1k
0
votes
0
replies
2.6k
views
Comment: C: File Containing LD-Pruned SNPs with MAF in CEU and YRI populations?
9.8 years ago by Katie D'Aco ★ 1.1k
0
votes
0
replies
3.8k
views
Comment: Comment: QC Sequence Data from VCF
updated 2.5 years ago by 43k • written 9.8 years ago by ★ 1.1k
0
votes
0
replies
3.4k
views
Comment: C: Machine learning procedure for cancer subtype discovery
9.8 years ago by Katie D'Aco ★ 1.1k
1
vote
0
replies
3.4k
views
Comment: Comment: Machine learning procedure for cancer subtype discovery
updated 2.5 years ago by 43k • written 9.8 years ago by ★ 1.1k
0
votes
1
reply
3.4k
views
Comment: C: SNP Questions: Mendelian Error Rates and SNP Orientation relative to genome.
9.9 years ago by Katie D'Aco ★ 1.1k
2
votes
0
replies
2.2k
views
Comment: C: Exome sequencing errors resulting in misdiagnosis?
9.9 years ago by Katie D'Aco ★ 1.1k
0
votes
1
reply
9.8k
views
Comment: C: Should I use MiSeq or HiSeq to generate data for assembling the bowfly genome?
9.9 years ago by Katie D'Aco ★ 1.1k
0
votes
0
replies
4.3k
views
Comment: C: remove private alleles from a vcf file
9.9 years ago by Katie D'Aco ★ 1.1k
0
votes
1
reply
4.3k
views
Comment: C: remove private alleles from a vcf file
9.9 years ago by Katie D'Aco ★ 1.1k
0
votes
0
replies
2.5k
views
Comment: C: PLINK 1.90 alpha
10.0 years ago by Katie D'Aco ★ 1.1k
1
vote
0
replies
15k
views
Comment: C: Extracting regions from .bam file using a .gff or .gtf file
10.0 years ago by Katie D'Aco ★ 1.1k
0
votes
0
replies
15k
views
Comment: C: Extracting regions from .bam file using a .gff or .gtf file
10.0 years ago by Katie D'Aco ★ 1.1k
39 results • Page 1 of 1
Content Search
Users
Tags
Badges
Help About
FAQ
Access RSS
API
Stats

Use of this site constitutes acceptance of our User Agreement and Privacy Policy.

Powered by the version 2.3.6