Profile Posts Awards
Show
all questions tools blogs news tutorials forum answers comments
Showing : questions
0
votes
2
replies
344
views
How to obtain Node/ Edge information from a Reactome Pathway
R API pathways reactome databases
updated 4 weeks ago by 141k • written 8 weeks ago by ▴ 140
0
votes
0
replies
365
views
How to read count information from an old RGB based Agilent DNA array
CNV Agilent DNA WGS
9 months ago by K.patel5 ▴ 140
1
vote
0
replies
330
views
Can ART be used to generate a WES .sam file rather than a WGS file?
genomics biology WGS synthetic WES
18 months ago by K.patel5 ▴ 140
1
vote
5
replies
752
views
Advice on how to generate synthetic Copy Number Variation data
CNV genomics biology synthetic WES
updated 18 months ago by ▴ 270 • written 18 months ago by ▴ 140
0
votes
1
reply
873
views
VEP/ CADD error - ERROR: Assembly is GRCh38 but CADD file does not contain GRCh38 in header.
CADD trio WES VEP
updated 11 months ago by ▴ 690 • written 20 months ago by ▴ 140
3
votes
4
replies
1.2k
views
How to add transcript and cpg site information to a bed file
genomics annotations cpg BED
19 months ago by K.patel5 ▴ 140
1
vote
2
replies
1.4k
views
How to pipe bcftools query to bcftools fill-tags
BCFtools variant-calling genomics
updated 10 months ago by 43k • written 2.1 years ago by ▴ 140
4
votes
3
replies
960
views
How to use BCFtools to keep variants if they are `DP > 10` in all samples?
BCFtools variant-calling genomics
updated 10 months ago by 43k • written 2.2 years ago by ▴ 140
7
votes
3
replies
2.0k
views
GATK4 - To be known or not to be known, that is the question.
WGS WES flags GATK
updated 2.3 years ago by 5.7k • written 2.3 years ago by ▴ 140
2
votes
3
replies
1.9k
views
VEP - How to retrieve information from the INFO column of a vcf file neatly
tab vcf annotations VEP
updated 2.2 years ago by 11k • written 2.3 years ago by ▴ 140
7
votes
4
replies
3.9k
views
How to create specific .bed files for a panel of genes
panel genomics BED
2.3 years ago by K.patel5 ▴ 140
4
votes
4
replies
1.9k
views
Attempting to generate a bam.bai file but the output is not readable
exome samtools sequencing BAM
2.4 years ago by K.patel5 ▴ 140
3
votes
2
replies
997
views
Is it necessary to test for multiple correction during differential expression analysis on microRNA data?
microRNA miRNA-seq differential expression stats
updated 3.2 years ago by 8.7k • written 3.2 years ago by ▴ 140
5
votes
6
replies
2.2k
views
How does miRdeep2 normalise sequences
miRNA sequencing miRDeep2
updated 2.7 years ago by ▴ 10 • written 3.4 years ago by ▴ 140
5
votes
4
replies
3.2k
views
Why do some gene set enrichment services do not ask for a background data set
enrichr panther GOrilla GSEA
4.2 years ago by K.patel5 ▴ 140
1
vote
2
replies
1.6k
views
Processing .raw files or out.tar files from Mass Spec
mass spec R proteomics
4.8 years ago by K.patel5 ▴ 140
7
votes
8
replies
1.6k
views
fastq dump usage of microRNA-seq data
RNA-Seq microRNA fastq
4.9 years ago by K.patel5 ▴ 140
8
votes
2
replies
3.3k
views
Removing low level expression genes from microarray experiments
next-gen microarray
updated 4.9 years ago by 35k • written 4.9 years ago by ▴ 140
18 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