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genomes
•
reset
0
votes
2
replies
2.7k
views
How to get the rsID of 4 million SNPA
ensembldb
SNP
SNPData
genomes
written 2.2 years ago by
Weiqiong
• 0
0
votes
0
replies
382
views
Job:
Bioinformatics Research Associate in Transcriptomics, Epigenomics and Multi-omics
genomes
6 months ago
JP Carter
▴ 40
0
votes
0
replies
377
views
Job:
Bioinformatics Research Associate, Genomics and Genetics
genomes
Genetics
6 months ago
JP Carter
▴ 40
1
vote
1
reply
423
views
MSc student
genomes
updated 16 months ago by
Basti
▴ 780 • written 16 months ago by
Deeplaxmi
• 0
0
votes
3
replies
4.9k
views
how to get gene list for given GO terms?
Pathways
GO
Cancer
PROcess
goTools
genomes
Pathways
GO
Cancer
PROcess
goTools
genomes
updated 22 months ago by
pengmin.wang.1
• 0 • written 12.2 years ago by
Marc Carlson
★ 7.2k
0
votes
0
replies
852
views
How to assign custom colour codes for Multiple sequence alignment (MSA)?
Phylogenetics
genomes
R
MultipleSequenceAlignment
Bioconductor
2.8 years ago • updated 2.7 years ago
K.
• 0
1
vote
0
replies
1.4k
views
Job:
Bioinformatician/Computational Biologist - Dublin City, Ireland
bioinformatician job
computational biology
genomes
pathways
machine learning
Job
6.6 years ago
bulfin.triona
▴ 10
0
votes
0
replies
988
views
How to generate CpG island Unmasked.bed file format for finding CpG island shores and shelves?
bioconductor
annotation
rtracklayer
genomes
homo.sapiens
6.9 years ago
sivabala76
• 0
0
votes
5
replies
1.4k
views
Extracting all possible annotations between two genomic coordinates
genomes
7.2 years ago
KB
▴ 50
0
votes
0
replies
1.1k
views
vizualization of mutations
genomes
SNP
7.7 years ago
Bogdan
▴ 670
0
votes
0
replies
1.7k
views
Job:
Postdoc / Computational Biologist for circulating tumor DNA/RNA profiling at Memorial Sloan Kettering Cancer Center MSKCC, New York
cancer
sequencing
genetics
genomes
diagnostic
Job
7.7 years ago
dtlabmskcc
• 0
1
vote
1
reply
1.7k
views
GenomeViz
Proteomics
genomes
Proteomics
genomes
updated 8.3 years ago by
xianxiu
• 0 • written 19.3 years ago by
Rohit Ghai
▴ 80
0
votes
1
reply
1.2k
views
Request: Add Macaca fascicularis genome to BSgenome
bsgenome
genomes
updated 9.0 years ago by
Hervé Pagès
16k • written 9.0 years ago by
amy.klegarth
• 0
0
votes
0
replies
1.6k
views
Job:
Harvard Medical School: Postdoctoral Opportunity
genomes
Job
9.6 years ago
Doe, Aimee
▴ 40
0
votes
8
replies
2.8k
views
Best practices to find intersection among variants
VariantAnnotation
genomes
VariantAnnotation
VariantAnnotation
genomes
VariantAnnotation
updated 9.7 years ago by
Julian Gehring
★ 1.3k • written 9.7 years ago by
Marco Blanchette
▴ 220
2
votes
3
replies
5.1k
views
Linkage disequilibrium with 1000 Genomes/HapMap
HapMap
genomes
HapMap
genomes
9.8 years ago
enricoferrero
▴ 660
0
votes
3
replies
1.5k
views
Elephant shark genome
Biostrings
genomes
Biostrings
genomes
updated 10.1 years ago by
Martin Morgan
25k • written 10.1 years ago by
Guest User
★ 13k
0
votes
1
reply
2.1k
views
It works! RE: So close, but still error: RE: Rsamtools filtering bam file: RE: MEDIPS.createSet error
Alignment
GO
Cancer
BSgenome
BSgenome
Rsamtools
genomes
MEDIPS
Alignment
GO
Cancer
updated 10.1 years ago by
Lukas Chavez
▴ 570 • written 10.1 years ago by
Vining, Kelly
▴ 220
0
votes
1
reply
1.6k
views
GOseq with ce6
GO
Yeast
Organism
goseq
genomes
GO
Yeast
Organism
goseq
genomes
updated 10.1 years ago by
Nadia Davidson
▴ 310 • written 10.1 years ago by
François Lefebvre
▴ 50
0
votes
0
replies
1.5k
views
Trying to use BSgenome.Hsapiens.NCBI.GRCh38
Cancer
BSgenome
BSgenome
genomes
Cancer
BSgenome
BSgenome
genomes
10.1 years ago
Hervé Pagès
16k
0
votes
1
reply
1.8k
views
So close, but still error: RE: Rsamtools filtering bam file: RE: MEDIPS.createSet error
Alignment
GO
Cancer
BSgenome
BSgenome
Rsamtools
genomes
MEDIPS
Alignment
GO
Cancer
updated 10.1 years ago by
Lukas Chavez
▴ 570 • written 10.1 years ago by
Vining, Kelly
▴ 220
0
votes
5
replies
2.0k
views
Rsamtools filtering bam file: RE: MEDIPS.createSet error
GO
BSgenome
BSgenome
Rsamtools
genomes
MEDIPS
GO
BSgenome
BSgenome
Rsamtools
genomes
updated 10.1 years ago by
Martin Morgan
25k • written 10.1 years ago by
Vining, Kelly
▴ 220
0
votes
3
replies
2.0k
views
Find enriched GO terms, given a list of GO terms of interest and background GO terms
Annotation
GO
topGO
genomes
Annotation
GO
topGO
genomes
10.3 years ago
Guest User
★ 13k
0
votes
1
reply
1.7k
views
makeTranscriptDbFromUCSC() error
genomes
genomes
10.3 years ago
Chris Cabanski
▴ 30
0
votes
2
replies
2.2k
views
ensemblVEP, variant_effect_predictor versions and release schedule
Transcription
HapMap
PolyPhen
SIFT
convert
genomes
ensemblVEP
Transcription
HapMap
SIFT
updated 10.4 years ago by
Valerie Obenchain
★ 6.8k • written 10.4 years ago by
Thomas Sandmann
▴ 30
0
votes
1
reply
2.3k
views
Pairwise Alignment on Large Protein Sequence Data Set
Alignment
genomes
Alignment
genomes
updated 10.4 years ago by
Hervé Pagès
16k • written 10.4 years ago by
Guest User
★ 13k
0
votes
0
replies
1.5k
views
Gviz and Leishmania genomes
rtracklayer
genomes
Gviz
rtracklayer
genomes
Gviz
10.5 years ago
florian.hahne@novartis.com
★ 1.6k
0
votes
0
replies
1.8k
views
Create a sample file /tab delimited file in QuasR
BSgenome
convert
BSgenome
genomes
QuasR
BSgenome
convert
BSgenome
genomes
QuasR
10.6 years ago
Michael Stadler
▴ 350
0
votes
1
reply
1.6k
views
makeTranscriptDbFromGFF fails on NCBI Bacteria genomes
GO
TranscriptDb
goseq
genomes
GO
TranscriptDb
goseq
genomes
updated 10.6 years ago by
Marc Carlson
★ 7.2k • written 10.6 years ago by
刘鹏飞
▴ 80
0
votes
1
reply
1.5k
views
Lifting over a bam file with Rsamtools and GenomicRanges
GenomicRanges
genomes
GenomicRanges
genomes
updated 10.7 years ago by
Michael Lawrence
★ 11k • written 10.7 years ago by
Guest User
★ 13k
0
votes
0
replies
1.2k
views
SnpStats - STRING_ELT() error and Fst
genomes
genomes
10.7 years ago
Voke AO
▴ 760
0
votes
1
reply
1.3k
views
Working with non-type strain annotation
Proteomics
GO
genomes
Proteomics
GO
genomes
updated 11.0 years ago by
Marc Carlson
★ 7.2k • written 11.0 years ago by
Thomas Lin Pedersen
▴ 70
0
votes
8
replies
3.2k
views
QuasR: how to use an indexed reference genome?
BSgenome
BSgenome
genomes
QuasR
BSgenome
BSgenome
genomes
QuasR
updated 11.0 years ago by
Michael Stadler
▴ 350 • written 11.0 years ago by
Paul Shannon
▴ 750
0
votes
2
replies
1.6k
views
QuasR special case alignment
Alignment
genomes
QuasR
Alignment
genomes
QuasR
updated 11.0 years ago by
Ugo Borello
▴ 340 • written 11.1 years ago by
Michael Stadler
▴ 350
0
votes
6
replies
1.6k
views
coverage on very large ReadGappedAlignmentsObject
Coverage
genomes
Coverage
genomes
updated 11.0 years ago by
Martin Morgan
25k • written 11.0 years ago by
Stefanie
▴ 360
0
votes
1
reply
1.9k
views
Help needed! What wrong with VariantAnnotation and TCGA vcfs
VariantAnnotation
genomes
VariantAnnotation
VariantAnnotation
genomes
VariantAnnotation
updated 11.1 years ago by
Martin Morgan
25k • written 11.1 years ago by
ying chen
▴ 340
0
votes
0
replies
1.5k
views
Useful information about Ensembl release 71 mart databases
zebrafish
PolyPhen
SIFT
affy
genomes
zebrafish
PolyPhen
SIFT
affy
genomes
11.1 years ago
Thomas Maurel
▴ 800
0
votes
0
replies
1.4k
views
Biostatistician position in London
Cancer
genomes
Cancer
genomes
11.1 years ago
Kathi Zarnack
▴ 110
0
votes
2
replies
1.5k
views
Limit on number of sequence files for forging a BSgenome
GO
Cancer
BSgenome
BSgenome
genomes
GO
Cancer
BSgenome
BSgenome
genomes
11.1 years ago
Hervé Pagès
16k
3
votes
4
replies
1.2k
views
Limit on number of sequence files for forging a BSgenome
BSgenome
BSgenome
genomes
BSgenome
BSgenome
genomes
updated 11.2 years ago by
Kasper Daniel Hansen
★ 6.5k • written 11.2 years ago by
Marco Blanchette
▴ 220
0
votes
2
replies
1.0k
views
Expected value of finding a sequence (Tim Smith)
genomes
genomes
updated 11.2 years ago by
Alvaro J. González
▴ 10 • written 11.2 years ago by
Alvaro J. González
▴ 80
0
votes
0
replies
1.3k
views
Help with Gviz \"IdeogramTrack\" and \"BioMartGeneTrackRegion\" commands
zebrafish
biomaRt
ideogram
genomes
zebrafish
biomaRt
ideogram
genomes
11.3 years ago
florian.hahne@novartis.com
★ 1.6k
0
votes
0
replies
1.2k
views
Useful information about Ensembl release 70 mart databases
genomes
genomes
11.3 years ago
Thomas Maurel
▴ 800
0
votes
3
replies
1.3k
views
VCF predictCoding(...) providing inconsistent results?
genomes
genomes
11.3 years ago
Murat Tasan
▴ 70
0
votes
3
replies
2.3k
views
seqlevels in VCF objects
BSgenome
BSgenome
genomes
BSgenome
BSgenome
genomes
updated 11.3 years ago by
Valerie Obenchain
★ 6.8k • written 11.3 years ago by
Murat Tasan
▴ 70
0
votes
2
replies
1.2k
views
Granges averaging
genomes
genomes
updated 11.6 years ago by
Hervé Pagès
16k • written 11.6 years ago by
Yannick Wurm
▴ 40
0
votes
2
replies
1.6k
views
VariantAnnotation: readVcf on nonmodel organism
Organism
genomes
Organism
genomes
updated 11.6 years ago by
Valerie Obenchain
★ 6.8k • written 11.6 years ago by
Yannick Wurm
▴ 40
0
votes
2
replies
1.6k
views
Building custom genome in MeDIPS
BSgenome
BSgenome
genomes
MEDIPS
BSgenome
BSgenome
genomes
MEDIPS
updated 11.7 years ago by
James W. MacDonald
65k • written 11.7 years ago by
Yan He
▴ 10
0
votes
0
replies
1.1k
views
regarding mapping package
Cancer
genomes
Rsubread
gmapR
Cancer
genomes
Rsubread
gmapR
11.7 years ago
Martin Morgan
25k
0
votes
1
reply
985
views
How to use cutome reference genome?
BSgenome
BSgenome
genomes
MEDIPS
BSgenome
BSgenome
genomes
MEDIPS
updated 11.7 years ago by
Kasper Daniel Hansen
★ 6.5k • written 11.7 years ago by
Guest User
★ 13k
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Judging from your MDS plot, cell types 1 and 2 look radically different, so it would make perfect sense to analyse them separately. There's…
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Removing samples from one group nevertheless changes the variance estimation (dispersion) for all comparisons. So you could have pushed one…
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Comment: Numerical differences in DESeq2 output depending on different design matrix cons
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If you restrict yourself to, say, genes with a baseMean > 50, are the numerical differences between the two designs significant?
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