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comments
2
votes
3
replies
1.0k
views
6 follow
How to summarize the expression of a gene when having expression data from different transcripts of that gene
rnaseq
expression
updated 22 months ago by
i.sudbery
20k • written 22 months ago by
jeni
▴ 90
0
votes
0
replies
449
views
SNV occuring 2 fold more in forward than in reverse reads should be filtered?
Variant-Calling
updated 8 months ago by
Ram
44k • written 2.9 years ago by
jeni
▴ 90
0
votes
1
reply
4.9k
views
Comment:
Comment: MAGERI: a software tool for calling rare variants and detecting circulating tumo
3.6 years ago by
jeni
▴ 90
11
votes
5
replies
8.5k
views
Remove supplementary alignments from a bam file
alignment
updated 3.8 years ago by
cianagalis
• 0 • written 4.7 years ago by
jeni
▴ 90
0
votes
1
reply
734
views
How to statistically determine if a mutation has an impact on expression individually for one patient
RNA-Seq
variant calling
3.9 years ago by
jeni
▴ 90
0
votes
1
reply
837
views
Comment:
C: Correct number of detected variants by coverage
4.1 years ago by
jeni
▴ 90
0
votes
3
replies
837
views
Correct number of detected variants by coverage
variant calling
4.1 years ago by
jeni
▴ 90
0
votes
0
replies
1.1k
views
Comment:
C: Differencial expression analysis between groups determined by two variables
4.2 years ago by
jeni
▴ 90
0
votes
3
replies
1.1k
views
Differencial expression analysis between groups determined by two variables
expression
microarray
clustering
4.2 years ago by
jeni
▴ 90
0
votes
1
reply
1.9k
views
Comment:
C: Does it make sense to transform expression data to zscore after performing RMA?
4.2 years ago by
jeni
▴ 90
0
votes
1
reply
1.9k
views
Comment:
C: Does it make sense to transform expression data to zscore after performing RMA?
4.2 years ago by
jeni
▴ 90
3
votes
6
replies
1.9k
views
Does it make sense to transform expression data to zscore after performing RMA?
microarray
expression
updated 2.6 years ago by
kountaydwivedi
• 0 • written 4.2 years ago by
jeni
▴ 90
0
votes
0
replies
781
views
Is it right to use a low amount of bumphunter permutations?
methylation
microarray
DMR
4.2 years ago by
jeni
▴ 90
0
votes
1
reply
3.2k
views
Comment:
C: HOMER hg19 not found in config.txt
4.2 years ago by
jeni
▴ 90
0
votes
0
replies
624
views
How to deal with SNPs and INDELs called in hypermutated regions?
variant calling
4.4 years ago by
jeni
▴ 90
0
votes
0
replies
683
views
Where to find a list of hypermutated regions for hg19 assembly?
variant calling
4.4 years ago by
jeni
▴ 90
2
votes
1
reply
1.3k
views
How to know which genes are favouring or inactivating a pathway in a gene set enrichment analysis
enrichment analysis
updated 4.4 years ago by
Papyrus
★ 3.0k • written 4.4 years ago by
jeni
▴ 90
0
votes
0
replies
1.1k
views
Reduce GRanges by different lengths of overlapping, deppending on each compared intervals
GRanges
4.5 years ago by
jeni
▴ 90
1
vote
3
replies
3.2k
views
HOMER hg19 not found in config.txt
HOMER
motif
finding
updated 3.3 years ago by
Sarah
• 0 • written 4.5 years ago by
jeni
▴ 90
0
votes
0
replies
1.6k
views
Comment:
C: Best practice to find regulatory motifs in a set of sequences
4.5 years ago by
jeni
▴ 90
0
votes
1
reply
1.6k
views
Comment:
C: Best practice to find regulatory motifs in a set of sequences
4.5 years ago by
jeni
▴ 90
0
votes
1
reply
1.6k
views
Comment:
C: Best practice to find regulatory motifs in a set of sequences
4.5 years ago by
jeni
▴ 90
3
votes
9
replies
1.6k
views
Best practice to find regulatory motifs in a set of sequences
regulatory
motif
finding
updated 4.5 years ago by
Mensur Dlakic
★ 28k • written 4.5 years ago by
jeni
▴ 90
0
votes
1
reply
1.6k
views
Comment:
C: Best practice to find regulatory motifs in a set of sequences
4.5 years ago by
jeni
▴ 90
0
votes
1
reply
1.4k
views
Comment:
C: Best way to call differencially methylated positions taking into account results
4.5 years ago by
jeni
▴ 90
3
votes
3
replies
1.4k
views
Best way to call differencially methylated positions taking into account results from both Beta and M values
methylation
updated 4.5 years ago by
Papyrus
★ 3.0k • written 4.5 years ago by
jeni
▴ 90
0
votes
1
reply
11k
views
Comment:
C: Beta-values, M-values and thresholds on effect size
4.5 years ago by
jeni
▴ 90
2
votes
5
replies
1.6k
views
VEP is returning MOTIF_NAME values not recognised by Ensembl
snp
Ensembl
VEP
updated 4.5 years ago by
Michal @Ensembl
▴ 270 • written 4.6 years ago by
jeni
▴ 90
0
votes
0
replies
887
views
Download all positions where a motif exist from the genome browser
genome
4.5 years ago by
jeni
▴ 90
0
votes
1
reply
1.6k
views
Comment:
C: VEP is returning MOTIF_NAME values not recognised by Ensembl
4.6 years ago by
jeni
▴ 90
0
votes
0
replies
904
views
Comment:
C: Pathways analysis taking into account the number of times a gene is present amon
4.6 years ago by
jeni
▴ 90
0
votes
1
reply
904
views
Comment:
C: Pathways analysis taking into account the number of times a gene is present amon
4.6 years ago by
jeni
▴ 90
0
votes
1
reply
904
views
Comment:
C: Pathways analysis taking into account the number of times a gene is present amon
4.6 years ago by
jeni
▴ 90
0
votes
6
replies
904
views
Pathways analysis taking into account the number of times a gene is present among several patients
snp
4.6 years ago by
jeni
▴ 90
0
votes
0
replies
1.0k
views
Comment:
C: filter_vep not properly filtering
4.6 years ago by
jeni
▴ 90
2
votes
2
replies
1.4k
views
Read genotype information with VariantAnnotation
SNP
R
vcf
Bioconductor
VariantAnnotation
updated 4.6 years ago by
benformatics
4.1k • written 4.6 years ago by
jeni
▴ 90
0
votes
2
replies
1.0k
views
filter_vep not properly filtering
snp
updated 4.6 years ago by
Ram
44k • written 4.6 years ago by
jeni
▴ 90
0
votes
0
replies
3.7k
views
Comment:
C: Parse VEP VCF with variantAnnotation
4.6 years ago by
jeni
▴ 90
5
votes
6
replies
3.7k
views
Parse VEP VCF with variantAnnotation
snp
R
4.6 years ago by
jeni
▴ 90
0
votes
0
replies
3.7k
views
Comment:
C: Parse VEP VCF with variantAnnotation
4.6 years ago by
jeni
▴ 90
0
votes
1
reply
1.7k
views
Comment:
C: Is it right to combine multiple runs downloaded from SRA?
4.7 years ago by
jeni
▴ 90
1
vote
4
replies
1.7k
views
Is it right to combine multiple runs downloaded from SRA?
next-gen
4.7 years ago by
jeni
▴ 90
0
votes
4
replies
813
views
How to remove reads supporting the same fragment that other reads support
Assembly
genome
4.7 years ago by
jeni
▴ 90
0
votes
0
replies
813
views
Comment:
C: How to remove reads supporting the same fragment that other reads support
4.7 years ago by
jeni
▴ 90
2
votes
6
replies
3.4k
views
Extract reads with insert size 0 from a bam file
alignment
updated 4.7 years ago by
Friederike
9.0k • written 4.7 years ago by
jeni
▴ 90
0
votes
0
replies
3.4k
views
Comment:
C: Extract reads with insert size 0 from a bam file
4.7 years ago by
jeni
▴ 90
0
votes
1
reply
3.4k
views
Comment:
C: Extract reads with insert size 0 from a bam file
4.7 years ago by
jeni
▴ 90
0
votes
0
replies
1.1k
views
Comment:
C: Transform genomic intervals to genomic positions in an R dataframe
updated 4.7 years ago by
Kevin Blighe
88k • written 4.7 years ago by
jeni
▴ 90
0
votes
1
reply
1.1k
views
Comment:
C: Transform genomic intervals to genomic positions in an R dataframe
4.8 years ago by
jeni
▴ 90
0
votes
5
replies
1.1k
views
Transform genomic intervals to genomic positions in an R dataframe
R
4.8 years ago by
jeni
▴ 90
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