Profile Posts Awards
Show
all questions tools blogs news tutorials forum answers comments
7
votes
3
replies
4.9k
views
How To Find Repeat Expansion Using Exome/Genome Sequencing Data?
repeats
updated 5.4 years ago by ▴ 40 • written 12.0 years ago by ▴ 800
0
votes
1
reply
3.7k
views
Comment: C: The "Rareness" Of Two Adjacent Nonsynonymous Mutations.
updated 5.8 years ago by 44k • written 12.2 years ago by ▴ 800
7
votes
6
replies
3.3k
views
1000Genome SV integrated map's power for SV filter
1000 genome project structural variation filter
updated 6.0 years ago by ▴ 110 • written 8.6 years ago by ▴ 800
2
votes
3
replies
2.4k
views
Choosing controls for structural variation detection
NGS SV 1000 genome project
updated 6.2 years ago by 44k • written 8.8 years ago by ▴ 800
12
votes
3
replies
4.3k
views
Pipeline of structural variation calling using multiple tools for multiple samples
structural variation 1000 genome project
updated 6.2 years ago by 44k • written 8.8 years ago by ▴ 800
4
votes
10
replies
10k
views
Questions about multithreading of BWA
bwa multithread
updated 6.2 years ago by 44k • written 8.7 years ago by ▴ 800
0
votes
1
reply
10k
views
Comment: C: Questions about multithreading of BWA
updated 6.2 years ago by 44k • written 8.7 years ago by ▴ 800
0
votes
1
reply
10k
views
Comment: C: Questions about multithreading of BWA
updated 6.2 years ago by 44k • written 8.7 years ago by ▴ 800
0
votes
1
reply
10k
views
Comment: C: Questions about multithreading of BWA
updated 6.2 years ago by 44k • written 8.7 years ago by ▴ 800
10
votes
6
replies
9.8k
views
How To Call Snp From .Ab1 Files Of Sanger Sequencing?
snp
updated 6.4 years ago by ▴ 10 • written 11.8 years ago by ▴ 800
0
votes
0
replies
3.3k
views
Comment: C: Deep learning for genetics model of polygenic complex disease.
7.7 years ago by michealsmith ▴ 800
0
votes
2
replies
3.3k
views
Deep learning for genetics model of polygenic complex disease.
Deep learning Machine learning disease genetics
updated 7.7 years ago by 8.7k • written 7.7 years ago by ▴ 800
0
votes
1
reply
2.8k
views
Comment: C: Abnormal pair orientation in RNA-seq data
7.7 years ago by michealsmith ▴ 800
0
votes
0
replies
2.8k
views
Comment: C: Abnormal pair orientation in RNA-seq data
7.7 years ago by michealsmith ▴ 800
0
votes
0
replies
2.8k
views
Comment: C: Abnormal pair orientation in RNA-seq data
7.7 years ago by michealsmith ▴ 800
2
votes
13
replies
2.8k
views
Abnormal pair orientation in RNA-seq data
RNA-Seq igv inversion
7.7 years ago by michealsmith ▴ 800
0
votes
1
reply
2.8k
views
Comment: C: Abnormal pair orientation in RNA-seq data
7.7 years ago by michealsmith ▴ 800
0
votes
0
replies
2.8k
views
Comment: C: Abnormal pair orientation in RNA-seq data
7.7 years ago by michealsmith ▴ 800
0
votes
1
reply
2.8k
views
Comment: C: Abnormal pair orientation in RNA-seq data
7.7 years ago by michealsmith ▴ 800
0
votes
0
replies
1.4k
views
Allele-specific quantification methods for short tandem repeats?
microsatellite pcr qpcr allele
8.1 years ago by michealsmith ▴ 800
5
votes
1
reply
1.8k
views
Gene length bias for ontology analysis.
gene ontology
updated 8.5 years ago by ★ 2.6k • written 8.6 years ago by ▴ 800
3
votes
6
replies
2.9k
views
Prioritize structural variation (SV) callings supported by multiple softwares
SV structural variation intersect
updated 8.5 years ago by ★ 2.6k • written 8.6 years ago by ▴ 800
0
votes
0
replies
9.1k
views
Comment: C: Indel Discovery Delly, Pindel, Samtools, Gatk
8.6 years ago by michealsmith ▴ 800
0
votes
1
reply
2.9k
views
Comment: C: Prioritize structural variation (SV) callings supported by multiple softwares
8.6 years ago by michealsmith ▴ 800
0
votes
0
replies
2.4k
views
Comment: C: Choosing controls for structural variation detection
8.6 years ago by michealsmith ▴ 800
0
votes
0
replies
2.9k
views
Comment: C: Prioritize structural variation (SV) callings supported by multiple softwares
8.6 years ago by michealsmith ▴ 800
0
votes
0
replies
6.7k
views
Comment: Comment: Bioinformatic jobs outside academia?
updated 2.7 years ago by 44k • written 8.6 years ago by ▴ 800
0
votes
0
replies
1.6k
views
Comment: C: Control gene size for gene enrichment study
8.6 years ago by michealsmith ▴ 800
2
votes
2
replies
1.6k
views
Control gene size for gene enrichment study
gene enrichment GO
8.6 years ago by michealsmith ▴ 800
0
votes
1
reply
4.6k
views
Comment: C: How to do gene enrichment analysis?
8.6 years ago by michealsmith ▴ 800
7
votes
6
replies
4.6k
views
How to do gene enrichment analysis?
GO gene enrichment
updated 8.7 years ago by ▴ 370 • written 8.7 years ago by ▴ 800
29
votes
5
replies
4.1k
views
Career Plan: Be A Dual Benchworker And Bioinformatician
bioinformatician
updated 8.7 years ago by ★ 1.5k • written 11.9 years ago by ▴ 800
0
votes
0
replies
2.3k
views
Comment: C: Possible to find bioinformatician postdoc if I only could use other's programs a
8.7 years ago by michealsmith ▴ 800
0
votes
0
replies
2.3k
views
Comment: C: Possible to find bioinformatician postdoc if I only could use other's programs a
8.7 years ago by michealsmith ▴ 800
21
votes
5
replies
2.3k
views
Possible to find bioinformatician postdoc if I only could use other's programs and run pipeline?
bioinformatician postdoc
updated 19 months ago by 44k • written 8.7 years ago by ▴ 800
0
votes
0
replies
2.4k
views
Comment: C: Choosing controls for structural variation detection
8.8 years ago by michealsmith ▴ 800
2
votes
3
replies
2.9k
views
Forum: Career plan---Bench+bioinformatics or pure bioinformatics?
career benchwork
updated 2.3 years ago by 44k • written 8.8 years ago by ▴ 800
9
votes
5
replies
7.4k
views
Database To Look For Tissue-Specific Transcript Expression Of The Same Gene.
transcript
updated 2.7 years ago by 44k • written 11.8 years ago by ▴ 800
4
votes
3
replies
1.8k
views
Statistics For Merging Different Approaches
updated 9.3 years ago by 20 • written 12.6 years ago by ▴ 800
3
votes
3
replies
4.4k
views
Ibd Calculation For Small Familial Pedigrees
updated 22 months ago by 44k • written 12.0 years ago by ▴ 800
1
vote
7
replies
4.0k
views
What Genetic Marker To Use To Infer Pedigree From Sequencing Data?
genetics
updated 22 months ago by 44k • written 12.4 years ago by ▴ 800
17
votes
8
replies
17k
views
7 follow
Select Certain Column From Vcf File
vcf
updated 2.8 years ago by 44k • written 12.6 years ago by ▴ 800
7
votes
4
replies
4.7k
views
Publicly Available Rna-Seq Data For Study Splicing Change In Human Brain
rna-seq splicing
updated 3.6 years ago by 44k • written 10.7 years ago by ▴ 800
27
votes
8
replies
10k
views
6 follow
Difference "./." vs "0/0" In VCF files
genotyping vcf
updated 3.1 years ago by 12k • written 12.6 years ago by ▴ 800
9
votes
7
replies
3.7k
views
The "Rareness" Of Two Adjacent Nonsynonymous Mutations.
mutation
updated 11.2 years ago by 20 • written 12.2 years ago by ▴ 800
2
votes
4
replies
4.9k
views
What Are Good Values For R^2 And D' For Linkage Disequilibrium
linkage
updated 11.3 years ago by ▴ 470 • written 11.3 years ago by ▴ 800
1
vote
2
replies
6.1k
views
Combine/Merge Two Phased Vcf Files For Plink Analysis
plink
updated 11.3 years ago by ▴ 740 • written 11.3 years ago by ▴ 800
2
votes
2
replies
4.9k
views
Bwa Alignment: Gap Vs Soft-Clipped Sequences
bwa
updated 11.4 years ago by 20 • written 12.5 years ago by ▴ 800
0
votes
0
replies
7.4k
views
Comment: Comment: Database To Look For Tissue-Specific Transcript Expression Of The Same Gene.
updated 2.7 years ago by 44k • written 11.8 years ago by ▴ 800
1
vote
0
replies
9.8k
views
Comment: C: How To Call Snp From .Ab1 Files Of Sanger Sequencing?
11.8 years ago by michealsmith ▴ 800
91 results • Page 1 of 2
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