Latest
Open
Jobs
Tutorials
Tags
About
FAQ
Community
Planet
New Post
Log In
New Post
Latest
Open
News
Jobs
Tutorials
Forum
Tags
Planet
Users
Log In
Sign Up
About
Profile
Posts
Awards
Show
all
questions
tools
blogs
news
tutorials
forum
answers
comments
Showing :
answers
1
vote
0
replies
518
views
Answer:
Answer: Reasonable number of mutations in a human cancer cell exome
2.0 years ago by
LauferVA
4.2k
0
votes
0
replies
605
views
Answer:
Answer: 3 group differential gene analysis
2.1 years ago by
LauferVA
4.2k
1
vote
2
replies
1.2k
views
Answer:
Answer: Why my `Percent duplicates` in a shallow sequencing is too high?
2.2 years ago by
LauferVA
4.2k
0
votes
1
reply
761
views
Answer:
Answer: low counts in DESeq2
2.2 years ago by
LauferVA
4.2k
1
vote
1
reply
823
views
Answer:
Answer: Genetic Model when running PCA
2.2 years ago by
LauferVA
4.2k
2
votes
1
reply
2.3k
views
Answer:
Answer: WGCNA HeatMap correlating modules and sample conditions
2.2 years ago by
LauferVA
4.2k
1
vote
0
replies
627
views
Answer:
Answer: Checking chromosome builds for genotyping data
2.2 years ago by
LauferVA
4.2k
0
votes
0
replies
453
views
Answer:
Answer: plink
2.2 years ago by
LauferVA
4.2k
0
votes
0
replies
452
views
Answer:
Answer: Sharing interactive Cytoscape networks
2.2 years ago by
LauferVA
4.2k
2
votes
0
replies
871
views
Answer:
Answer: Alternatives to TMM normalization
2.2 years ago by
LauferVA
4.2k
0
votes
0
replies
497
views
Answer:
Answer: Batch effect
2.2 years ago by
LauferVA
4.2k
0
votes
0
replies
581
views
Answer:
Answer: Info/r2 threshold to use for LD file for FINEMAP/SUSIE
2.2 years ago by
LauferVA
4.2k
3
votes
1
reply
1.7k
views
Answer:
Answer: How to do pathway enrichment analysis with genomic ranges data (ATAC-Seq peaks)?
2.2 years ago by
LauferVA
4.2k
1
vote
0
replies
1.3k
views
Answer:
Answer: Weird QQ plot in GWAS analysis
2.2 years ago by
LauferVA
4.2k
0
votes
0
replies
525
views
Answer:
Answer: Can a heterogenous approach to data normalization yield a better consensus learn
2.3 years ago by
LauferVA
4.2k
0
votes
0
replies
1.3k
views
Answer:
Answer: Batch effect correction for bulk RNA-seq
2.3 years ago by
LauferVA
4.2k
0
votes
1
reply
1.7k
views
Answer:
Answer: Re-assembly assembled genomes
2.3 years ago by
LauferVA
4.2k
0
votes
0
replies
656
views
Answer:
Answer: DESEQ for Differential Expression
2.3 years ago by
LauferVA
4.2k
3
votes
1
reply
2.6k
views
Answer:
Answer: How to calculate the absolute p-value for GSEA which returned 0.0 as the p-value
2.3 years ago by
LauferVA
4.2k
6
votes
0
replies
1.4k
views
Answer:
Answer: Are the upregulated genes in one comparison the downregulated genes in the inver
2.3 years ago by
LauferVA
4.2k
0
votes
1
reply
1.2k
views
Answer:
Answer: How can I extract part of the DNA sequences that align to a specific region in t
2.3 years ago by
LauferVA
4.2k
0
votes
0
replies
645
views
Answer:
Answer: 4C packages
2.3 years ago by
LauferVA
4.2k
2
votes
1
reply
1.9k
views
Answer:
Answer: bioinformatics pipelines on GCP or AWS
2.1 years ago by
LauferVA
4.2k
3
votes
1
reply
1.6k
views
Answer:
Answer: DESeq2 normalization
2.3 years ago by
LauferVA
4.2k
1
vote
1
reply
3.3k
views
Answer:
Answer: Volcano plot
2.4 years ago by
LauferVA
4.2k
2
votes
1
reply
763
views
Answer:
Answer: CNV and frameshift change
2.4 years ago by
LauferVA
4.2k
0
votes
1
reply
2.3k
views
Answer:
Answer: Problem getting soft threshold power using WGCNA for RNA-seq data
2.5 years ago by
LauferVA
4.2k
0
votes
1
reply
989
views
Answer:
Answer: Assessing how similar/ different of activated pathways between multiple groups o
2.8 years ago by
LauferVA
4.2k
1
vote
0
replies
1.1k
views
Answer:
Answer: Variant Calling Heterozygous Reference Alleles
2.8 years ago by
LauferVA
4.2k
1
vote
1
reply
4.2k
views
Answer:
Answer: weird MAplot or volcano plot of DESeq2 diff result
2.8 years ago by
LauferVA
4.2k
1
vote
1
reply
1.2k
views
Answer:
Answer: Advice on organizing large GSVA heatmap
2.8 years ago by
LauferVA
4.2k
5
votes
1
reply
1.1k
views
Answer:
Answer: proportion of variance
2.8 years ago by
LauferVA
4.2k
0
votes
1
reply
1.3k
views
Answer:
Answer: is local ancestry inference typically always run w/ array genotypes instead of
2.8 years ago by
LauferVA
4.2k
3
votes
1
reply
1.1k
views
Answer:
Answer: population stratification for candidate gene association study
2.9 years ago by
LauferVA
4.2k
2
votes
0
replies
763
views
Answer:
Answer: Genotype imputation - do SNP IDs of input files and reference panels matter?
2.9 years ago by
LauferVA
4.2k
2
votes
1
reply
1.2k
views
Answer:
Answer: IMPUTE2 minimal number of SNPs per chunk
2.9 years ago by
LauferVA
4.2k
0
votes
0
replies
620
views
Answer:
Answer: IMPUTE2 limit to only one population of 1000G Reference
2.9 years ago by
LauferVA
4.2k
1
vote
1
reply
1.9k
views
Answer:
Answer: Visualizing the gene network obtained by WGCNA
2.9 years ago by
LauferVA
4.2k
6
votes
0
replies
3.5k
views
Answer:
A: GWAS data from an Illumina Omni express Array and Illumina 660 W Quad Array
updated 4.3 years ago by
Ram
43k • written 8.3 years ago by
LauferVA
4.2k
2
votes
0
replies
2.8k
views
Answer:
A: Principal component analyses
updated 4.5 years ago by
Ram
43k • written 8.7 years ago by
LauferVA
4.2k
3
votes
0
replies
5.9k
views
Answer:
A: Delete Text between two strings sed, awk
updated 4.5 years ago by
Ram
43k • written 8.8 years ago by
LauferVA
4.2k
1
vote
1
reply
1.8k
views
Answer:
A: Conditional motif enrichment in sequence and selex data
updated 4.5 years ago by
Ram
43k • written 8.8 years ago by
LauferVA
4.2k
3
votes
1
reply
4.1k
views
Answer:
A: Whole exome sequencing data, rare variants and QQ-plots
updated 5.6 years ago by
zx8754
11k • written 8.0 years ago by
LauferVA
4.2k
2
votes
1
reply
4.1k
views
Answer:
C: Whole exome sequencing data, rare variants and QQ-plots
updated 5.6 years ago by
zx8754
11k • written 8.0 years ago by
LauferVA
4.2k
2
votes
0
replies
4.1k
views
Answer:
A: Should I include multi-mapped reads for analysis that does not require significa
5.8 years ago by
LauferVA
4.2k
0
votes
0
replies
1.4k
views
Answer:
A: SNP tools to infer copy number variations (CNVs)
7.0 years ago by
LauferVA
4.2k
4
votes
1
reply
2.5k
views
Answer:
A: Identify recessive conditions from VCF files
7.0 years ago by
LauferVA
4.2k
2
votes
1
reply
3.9k
views
Answer:
A: Is it more correct to use r2 or D' for selecting SNPs in LD?
7.0 years ago by
LauferVA
4.2k
1
vote
0
replies
2.2k
views
Answer:
A: Limiting variants from WGS to GWAS regions to get more significant cis/trans eQT
7.0 years ago by
LauferVA
4.2k
5
votes
0
replies
5.2k
views
Answer:
A: errors in running smartpca
7.2 years ago by
LauferVA
4.2k
168 results • Page
3 of 4
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