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90
votes
44
replies
62k
views
28 follow
Tool to generate proportional Venn Diagrams?
visualization
updated 2.6 years ago by 44k • written 13.6 years ago by ★ 3.4k
0
votes
0
replies
25k
views
Comment: C: Converting Ensembl Gene Ids To Hgnc Gene Name / Coordinates
updated 5.0 years ago by 44k • written 13.0 years ago by ★ 3.4k
0
votes
0
replies
25k
views
Comment: C: Converting Ensembl Gene Ids To Hgnc Gene Name / Coordinates
updated 5.0 years ago by 44k • written 13.0 years ago by ★ 3.4k
0
votes
0
replies
25k
views
Comment: C: Converting Ensembl Gene Ids To Hgnc Gene Name / Coordinates
updated 5.0 years ago by 44k • written 13.0 years ago by ★ 3.4k
0
votes
0
replies
3.4k
views
Comment: C: Clinical Covariates And Level 1 Data In The Cancer Genome Atlas (Tcga)
updated 5.1 years ago by 44k • written 12.8 years ago by ★ 3.4k
0
votes
0
replies
62k
views
Comment: C: Tool To Generate Proportional Venn Diagrams?
updated 5.2 years ago by 44k • written 13.6 years ago by ★ 3.4k
5
votes
1
reply
5.6k
views
Answer: A: Conversion Of Pfb Files From Hg18 To Hg19
updated 5.2 years ago by 44k • written 12.9 years ago by ★ 3.4k
3
votes
1
reply
2.9k
views
Answer: A: Downloading Snps Which Failed Hardy-Weinberg From Hapmap Or 1000G Data
updated 5.2 years ago by 44k • written 13.0 years ago by ★ 3.4k
4
votes
0
replies
3.4k
views
Answer: A: Cnv Detection - Alignment Files With Reported Cnv Needed
updated 5.2 years ago by 44k • written 13.0 years ago by ★ 3.4k
4
votes
1
reply
7.7k
views
Answer: A: How To Get The Omim Id For A Dbsnp Entry
updated 5.2 years ago by 44k • written 13.8 years ago by ★ 3.4k
0
votes
0
replies
10k
views
Comment: C: Getting The Ld Data For The 1000 Genomes
updated 5.2 years ago by 44k • written 14.1 years ago by ★ 3.4k
2
votes
2
replies
7.9k
views
Answer: A: How To Find The List Of All Coding Snps / Exomic Variants In A Given Gene ?
updated 5.2 years ago by 44k • written 13.8 years ago by ★ 3.4k
0
votes
0
replies
41k
views
Comment: C: 1000 Genomes Ld Calculation
updated 5.2 years ago by 44k • written 14.1 years ago by ★ 3.4k
2
votes
0
replies
41k
views
Comment: C: 1000 Genomes Ld Calculation
updated 5.2 years ago by 44k • written 12.8 years ago by ★ 3.4k
12
votes
9
replies
41k
views
Answer: A: 1000 Genomes Ld Calculation
updated 5.2 years ago by 44k • written 12.9 years ago by ★ 3.4k
0
votes
0
replies
41k
views
Comment: C: 1000 Genomes Ld Calculation
updated 5.2 years ago by 44k • written 14.1 years ago by ★ 3.4k
1
vote
0
replies
3.0k
views
Linking Icd-9 Codes And Keywords With Disease Genes
cnv disease association
updated 5.8 years ago by 20 • written 10.8 years ago by ★ 3.4k
31
votes
10
replies
4.5k
views
6 follow
Determining Which New Snps In 1000G Data Result In Coding Changes
genome linkage alignment protein prediction
updated 5.9 years ago by 20 • written 14.1 years ago by ★ 3.4k
32
votes
19
replies
25k
views
9 follow
Converting Ensembl Gene Ids To Hgnc Gene Name / Coordinates
ensembl ucsc genome mapping coordinates
updated 6.9 years ago by ▴ 20 • written 13.0 years ago by ★ 3.4k
2
votes
2
replies
3.8k
views
Renaming SNPs or SNP matching
bedtools vcf exome-chip bim SNP
updated 2.8 years ago by 44k • written 10.2 years ago by ★ 3.4k
16
votes
9
replies
6.2k
views
Long Range Linkage Disequilibrium Between Snps
linkage snp
updated 8.5 years ago by ▴ 40 • written 12.9 years ago by ★ 3.4k
7
votes
6
replies
5.5k
views
Plotting Cnv Association And Gwas Association In A Single Plot
cnv gwas visualization
updated 9.1 years ago by 20 • written 13.2 years ago by ★ 3.4k
8
votes
5
replies
3.0k
views
Genotyping Costs Over Time
genotyping
updated 9.3 years ago by 20 • written 12.8 years ago by ★ 3.4k
11
votes
4
replies
2.6k
views
Investigating Synthetic Associations
association gwas non
updated 9.6 years ago by 20 • written 13.1 years ago by ★ 3.4k
0
votes
0
replies
2.0k
views
Comment: C: Comparing CNAs from two groups
10.2 years ago by Ryan D ★ 3.4k
0
votes
1
reply
7.8k
views
Comment: C: PLINK returns NA values for all minor allele frequencies in my data
10.2 years ago by Ryan D ★ 3.4k
2
votes
1
reply
27k
views
Comment: C: What Is The Importance Of The Hardy Weinberg Equilibrium In Gwas?
10.2 years ago by Ryan D ★ 3.4k
0
votes
1
reply
2.6k
views
Easiest way to determine copy number for all SVs in all samples in 1000 Genomes
SV CNV 1000 Genomes PLINK structural-variants
updated 2.9 years ago by 44k • written 10.3 years ago by ★ 3.4k
0
votes
0
replies
2.6k
views
Comment: Comment: Easiest way to determine copy number for all SVs in all samples in 1000 Genomes
updated 2.9 years ago by 44k • written 10.3 years ago by ★ 3.4k
18
votes
6
replies
5.1k
views
Resequencing Genes/Regions Identified By Gwas
gwas linkage next-gen sequencing
updated 10.6 years ago by 20 • written 13.8 years ago by ★ 3.4k
0
votes
0
replies
4.3k
views
Comment: C: How To Get Full Information About Rna-Seq File?
10.6 years ago by Ryan D ★ 3.4k
6
votes
1
reply
9.5k
views
Answer: A: Cnv Annotation Tools
10.6 years ago by Ryan D ★ 3.4k
1
vote
0
replies
4.2k
views
Answer: A: Cnv Data
10.6 years ago by Ryan D ★ 3.4k
0
votes
0
replies
5.5k
views
Answer: A: Tools For Analyzing Copy Number Variation On All-Tumor Exome-Seq Samples
10.6 years ago by Ryan D ★ 3.4k
1
vote
0
replies
9.5k
views
Comment: C: Cnv Annotation Tools
10.6 years ago by Ryan D ★ 3.4k
0
votes
0
replies
5.8k
views
Answer: A: Changing Build From 37 To 36 In Snp Data
10.7 years ago by Ryan D ★ 3.4k
88
votes
36
replies
41k
views
15 follow
1000 Genomes Ld Calculation
genome linkage gwas
updated 10.7 years ago by ▴ 970 • written 14.1 years ago by ★ 3.4k
6
votes
3
replies
5.4k
views
Using Tabix And Vcf Tools To Get Cnv / Sv Frequencies From 1000 Genomes Data
genome tabix vcftools cnv
updated 10.8 years ago by 20 • written 13.0 years ago by ★ 3.4k
2
votes
1
reply
14k
views
Answer: A: Renaming All Files In A Directory With A Perl Script
10.8 years ago by Ryan D ★ 3.4k
3
votes
1
reply
8.7k
views
Answer: A: Strange Gene Ids In Tcga
10.8 years ago by Ryan D ★ 3.4k
1
vote
0
replies
8.7k
views
Comment: C: Strange Gene Ids In Tcga
10.8 years ago by Ryan D ★ 3.4k
14
votes
9
replies
4.5k
views
Finding An Genomic Intervals Shared For A Given Individual As Called By Two Or More Algorithms
galaxy clustering
updated 10.9 years ago by 20 • written 13.0 years ago by ★ 3.4k
0
votes
0
replies
10k
views
Comment: C: Cnv Calling Methods For The Illumina Omni2.5 - Penncnv And Quantisnp Possible?
11.2 years ago by Ryan D ★ 3.4k
10
votes
2
replies
3.0k
views
Removing Low Quality Lof Variants From 1000 Genomes Imputation
genome imputation snp mutation error
updated 11.2 years ago by 20 • written 12.7 years ago by ★ 3.4k
6
votes
31
replies
10k
views
16 follow
Cnv Calling Methods For The Illumina Omni2.5 - Penncnv And Quantisnp Possible?
cnv illumina copynumber
updated 11.3 years ago by • 0 • written 13.2 years ago by ★ 3.4k
0
votes
1
reply
17k
views
Comment: C: How To Process The Cnv Level 3 Data From Tcga
11.5 years ago by Ryan D ★ 3.4k
0
votes
1
reply
3.7k
views
Comment: C: Using Snps To Tag Deletions In 1000 Genomes
11.5 years ago by Ryan D ★ 3.4k
5
votes
2
replies
17k
views
Answer: A: How To Process The Cnv Level 3 Data From Tcga
11.5 years ago by Ryan D ★ 3.4k
0
votes
1
reply
3.7k
views
Comment: C: Using Snps To Tag Deletions In 1000 Genomes
11.5 years ago by Ryan D ★ 3.4k
1
vote
0
replies
7.6k
views
Answer: A: Tools For Pathway/Gene Set Analysis Of Gwas (Genome-Wide Association Study) Data
11.5 years ago by Ryan D ★ 3.4k
174 results • Page 1 of 4
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