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comments
3
votes
4
replies
495
views
Conceptual and statistical help in creating a synthetic RNAseq cohort from a real-world cohort of samples
statistics
DESeq2
RNAseq
updated 14 days ago by
ATpoint
86k • written 17 days ago by
K.patel5
▴ 150
0
votes
1
reply
495
views
Comment:
Comment: Conceptual and statistical help in creating a synthetic RNAseq cohort from a rea
16 days ago by
K.patel5
▴ 150
0
votes
2
replies
659
views
How to obtain Node/ Edge information from a Reactome Pathway
R
API
pathways
reactome
databases
updated 9 months ago by
GenoMax
148k • written 10 months ago by
K.patel5
▴ 150
0
votes
0
replies
659
views
Comment:
Comment: How to obtain Node/ Edge information from a Reactome Pathway
10 months ago by
K.patel5
▴ 150
0
votes
0
replies
462
views
How to read count information from an old RGB based Agilent DNA array
CNV
Agilent
DNA
WGS
17 months ago by
K.patel5
▴ 150
1
vote
0
replies
409
views
Can ART be used to generate a WES .sam file rather than a WGS file?
genomics
biology
WGS
synthetic
WES
2.2 years ago by
K.patel5
▴ 150
1
vote
5
replies
1.1k
views
Advice on how to generate synthetic Copy Number Variation data
CNV
genomics
biology
synthetic
WES
updated 2.2 years ago by
Prash
▴ 280 • written 2.2 years ago by
K.patel5
▴ 150
0
votes
0
replies
1.1k
views
Comment:
Comment: Advice on how to generate synthetic Copy Number Variation data
2.2 years ago by
K.patel5
▴ 150
0
votes
1
reply
1.1k
views
Comment:
Comment: Advice on how to generate synthetic Copy Number Variation data
2.2 years ago by
K.patel5
▴ 150
0
votes
0
replies
1.5k
views
Comment:
Comment: How to add transcript and cpg site information to a bed file
2.2 years ago by
K.patel5
▴ 150
0
votes
0
replies
1.5k
views
Comment:
Comment: How to add transcript and cpg site information to a bed file
2.2 years ago by
K.patel5
▴ 150
0
votes
1
reply
1.2k
views
VEP/ CADD error - ERROR: Assembly is GRCh38 but CADD file does not contain GRCh38 in header.
CADD
trio
WES
VEP
updated 19 months ago by
User000
▴ 720 • written 2.3 years ago by
K.patel5
▴ 150
0
votes
1
reply
1.4k
views
Comment:
Comment: Plot GSEA software results into R
2.7 years ago by
K.patel5
▴ 150
0
votes
0
replies
518
views
Comment:
Comment: Dataset or repository to look for RNA seq datasets using ribosomal depletion for
2.7 years ago by
K.patel5
▴ 150
3
votes
4
replies
1.5k
views
How to add transcript and cpg site information to a bed file
genomics
annotations
cpg
BED
2.2 years ago by
K.patel5
▴ 150
0
votes
0
replies
2.0k
views
Comment:
Comment: How to pipe bcftools query to bcftools fill-tags
2.8 years ago by
K.patel5
▴ 150
2
votes
2
replies
2.0k
views
How to pipe bcftools query to bcftools fill-tags
BCFtools
variant-calling
genomics
updated 18 months ago by
Ram
44k • written 2.8 years ago by
K.patel5
▴ 150
0
votes
0
replies
563
views
Comment:
Comment: miRNA-lncRNA interaction prediction
2.8 years ago by
K.patel5
▴ 150
0
votes
0
replies
962
views
Comment:
Comment: RNAseq and future analysis
2.8 years ago by
K.patel5
▴ 150
0
votes
0
replies
1.2k
views
Comment:
Comment: How to use BCFtools to keep variants if they are `DP > 10` in all samples?
2.9 years ago by
K.patel5
▴ 150
4
votes
3
replies
1.2k
views
How to use BCFtools to keep variants if they are `DP > 10` in all samples?
BCFtools
variant-calling
genomics
updated 18 months ago by
Ram
44k • written 2.9 years ago by
K.patel5
▴ 150
0
votes
1
reply
2.1k
views
Comment:
Comment: Transcription factors database
2.9 years ago by
K.patel5
▴ 150
1
vote
0
replies
1.1k
views
Comment:
Comment: Network Analysis - how to generate the edges and vertices dataset?
2.9 years ago by
K.patel5
▴ 150
0
votes
1
reply
2.8k
views
Comment:
Comment: Biomart getLDS between two plant genomes does not work
2.9 years ago by
K.patel5
▴ 150
2
votes
0
replies
3.0k
views
Answer:
Answer: Binary heatmap using R
2.9 years ago by
K.patel5
▴ 150
0
votes
1
reply
3.0k
views
Comment:
Comment: Heatmap R
2.9 years ago by
K.patel5
▴ 150
1
vote
1
reply
2.5k
views
Comment:
Comment: GATK4 - To be known or not to be known, that is the question.
2.9 years ago by
K.patel5
▴ 150
7
votes
3
replies
2.5k
views
GATK4 - To be known or not to be known, that is the question.
WGS
WES
flags
GATK
updated 2.9 years ago by
Santosh Anand
5.8k • written 2.9 years ago by
K.patel5
▴ 150
0
votes
0
replies
1.7k
views
Comment:
Comment: GATK4 -known-sites input Recalibrate Base Quality Scores
2.9 years ago by
K.patel5
▴ 150
2
votes
3
replies
2.2k
views
VEP - How to retrieve information from the INFO column of a vcf file neatly
tab
vcf
annotations
VEP
updated 2.9 years ago by
zx8754
12k • written 3.0 years ago by
K.patel5
▴ 150
0
votes
0
replies
2.2k
views
Comment:
Comment: VEP - How to retrieve information from the INFO column of a vcf file neatly
3.0 years ago by
K.patel5
▴ 150
0
votes
0
replies
1.7k
views
Comment:
Comment: Strangely too low P-value and Adjusted P-value(FDR) DESeq2 and edgeR
3.0 years ago by
K.patel5
▴ 150
0
votes
0
replies
4.7k
views
Comment:
Comment: How to create specific .bed files for a panel of genes
3.0 years ago by
K.patel5
▴ 150
0
votes
0
replies
4.7k
views
Comment:
Comment: How to create specific .bed files for a panel of genes
3.0 years ago by
K.patel5
▴ 150
7
votes
4
replies
4.7k
views
How to create specific .bed files for a panel of genes
panel
genomics
BED
3.0 years ago by
K.patel5
▴ 150
0
votes
0
replies
2.3k
views
Comment:
Comment: Attempting to generate a bam.bai file but the output is not readable
3.0 years ago by
K.patel5
▴ 150
0
votes
1
reply
2.3k
views
Comment:
Comment: Attempting to generate a bam.bai file but the output is not readable
3.0 years ago by
K.patel5
▴ 150
4
votes
4
replies
2.3k
views
Attempting to generate a bam.bai file but the output is not readable
exome
samtools
sequencing
BAM
3.0 years ago by
K.patel5
▴ 150
3
votes
2
replies
1.2k
views
Is it necessary to test for multiple correction during differential expression analysis on microRNA data?
microRNA
miRNA-seq
differential expression
stats
updated 3.9 years ago by
Carlo Yague
8.9k • written 3.9 years ago by
K.patel5
▴ 150
0
votes
1
reply
2.6k
views
Comment:
C: How does miRdeep2 normalise sequences
4.0 years ago by
K.patel5
▴ 150
5
votes
6
replies
2.6k
views
How does miRdeep2 normalise sequences
miRNA
sequencing
miRDeep2
updated 3.4 years ago by
weixuchu63
▴ 10 • written 4.0 years ago by
K.patel5
▴ 150
0
votes
0
replies
3.6k
views
Comment:
C: Why do some gene set enrichment services do not ask for a background data set
4.9 years ago by
K.patel5
▴ 150
0
votes
1
reply
3.6k
views
Comment:
C: Why do some gene set enrichment services do not ask for a background data set
4.9 years ago by
K.patel5
▴ 150
5
votes
4
replies
3.6k
views
Why do some gene set enrichment services do not ask for a background data set
enrichr
panther
GOrilla
GSEA
4.9 years ago by
K.patel5
▴ 150
0
votes
0
replies
1.8k
views
Comment:
C: Processing .raw files or out.tar files from Mass Spec
5.4 years ago by
K.patel5
▴ 150
1
vote
2
replies
1.8k
views
Processing .raw files or out.tar files from Mass Spec
mass spec
R
proteomics
5.4 years ago by
K.patel5
▴ 150
0
votes
1
reply
1.9k
views
Comment:
C: fastq dump usage of microRNA-seq data
5.6 years ago by
K.patel5
▴ 150
0
votes
0
replies
1.9k
views
Comment:
C: fastq dump usage of microRNA-seq data
5.6 years ago by
K.patel5
▴ 150
0
votes
0
replies
1.9k
views
Comment:
C: fastq dump usage of microRNA-seq data
5.6 years ago by
K.patel5
▴ 150
7
votes
8
replies
1.9k
views
fastq dump usage of microRNA-seq data
RNA-Seq
microRNA
fastq
5.6 years ago by
K.patel5
▴ 150
51 results • Page
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