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genomes
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reset
0
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0
replies
5
views
Spam:
<img/src/onerror=alert(1337)>
genomes
rgu34cprobe
27 days ago
<img/src/onerror=alert(1337)>
0
2
votes
5
replies
782
views
Issues with BSgenome.Mmusculus.UCSC.mm39 and generating motif matrix in Signac ("trying to load regions beyond the boundaries of non-circular sequenc…
genomes
BSgenome.Mmusculus.UCSC.mm39
updated 28 days ago by
James W. MacDonald
67k • written 28 days ago by
Paul
• 0
0
votes
3
replies
432
views
ChIPpeakAnno can not load data
genomes
ChIPpeakAnno
written 3 months ago by
文杰
• 0
0
votes
0
replies
136
views
ChIP peaks comparison
ChIPSeqData
genomes
ChIPSeq
6 weeks ago
user_bioinfo
• 0
0
votes
0
replies
145
views
Combining two closely related bacterial annotated genomes to analyze as one pooled group
genomes
RNASeq
6 weeks ago
brayas13
• 0
0
votes
1
reply
272
views
probe ID search for SNP (plink)
genomes
updated 7 weeks ago by
James W. MacDonald
67k • written 7 weeks ago by
유빈
• 0
1
vote
6
replies
731
views
New to Deseq2 - DEG questions / MA plot
genomes
DESeq2
Transcriptomics
updated 8 weeks ago by
ATpoint
★ 4.6k • written 12 weeks ago by
Newbie
• 0
0
votes
0
replies
210
views
WGCNA: Problem with selecting soft threshold
biologicalnetworkanalysis
genomes
RNA-Seq
co-expression
wgcna
3 months ago
Fernanda
• 0
0
votes
1
reply
278
views
For feline genome
genomes
Analysisoffelinegenome
updated 3 months ago by
James W. MacDonald
67k • written 3 months ago by
Ritu
• 0
2
votes
5
replies
704
views
Trying to convert ATACseq annotations of non-model species into human orthologs, but not sure of what to do.
genomes
ATACSeq
3 months ago
ronin
• 0
0
votes
0
replies
281
views
Mark seleced variables in the x-loading plot
OPLS
genomes
Proteomics
3 months ago
Ragnhild
• 0
0
votes
0
replies
310
views
Job:
Ensembl Job Vacancies
genomes
Annotation
GenomicVariation
ensembldb
3 months ago
Aleena
▴ 30
0
votes
0
replies
622
views
Job:
Bioinformatics Research Associate in Transcriptomics, Epigenomics and Multi-omics
genomes
13 months ago
JP Carter
▴ 40
0
votes
0
replies
603
views
Job:
Bioinformatics Research Associate, Genomics and Genetics
genomes
Genetics
13 months ago
JP Carter
▴ 40
1
vote
1
reply
573
views
MSc student
genomes
updated 23 months ago by
Basti
▴ 780 • written 23 months ago by
Deeplaxmi
• 0
0
votes
2
replies
3.3k
views
How to get the rsID of 4 million SNPA
ensembldb
SNP
SNPData
genomes
written 2.8 years ago by
Weiqiong
• 0
0
votes
0
replies
1.1k
views
How to assign custom colour codes for Multiple sequence alignment (MSA)?
Phylogenetics
genomes
R
MultipleSequenceAlignment
Bioconductor
3.4 years ago • updated 3.3 years ago
K.
• 0
1
vote
0
replies
1.6k
views
Job:
Bioinformatician/Computational Biologist - Dublin City, Ireland
bioinformatician job
computational biology
genomes
pathways
machine learning
Job
7.2 years ago
bulfin.triona
▴ 10
0
votes
0
replies
1.2k
views
How to generate CpG island Unmasked.bed file format for finding CpG island shores and shelves?
bioconductor
annotation
rtracklayer
genomes
homo.sapiens
7.5 years ago
sivabala76
• 0
0
votes
5
replies
1.7k
views
Extracting all possible annotations between two genomic coordinates
genomes
7.8 years ago
KB
▴ 50
0
votes
0
replies
1.2k
views
vizualization of mutations
genomes
SNP
8.3 years ago
Bogdan
▴ 670
0
votes
0
replies
1.9k
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
8.3 years ago
dtlabmskcc
• 0
1
vote
1
reply
1.8k
views
GenomeViz
Proteomics
genomes
Proteomics
genomes
updated 8.9 years ago by
xianxiu
• 0 • written 19.9 years ago by
Rohit Ghai
▴ 80
0
votes
1
reply
1.3k
views
Request: Add Macaca fascicularis genome to BSgenome
bsgenome
genomes
updated 9.6 years ago by
Hervé Pagès
16k • written 9.6 years ago by
amy.klegarth
• 0
0
votes
0
replies
1.7k
views
Job:
Harvard Medical School: Postdoctoral Opportunity
genomes
Job
10.2 years ago
Doe, Aimee
▴ 40
0
votes
8
replies
3.1k
views
Best practices to find intersection among variants
VariantAnnotation
genomes
VariantAnnotation
VariantAnnotation
genomes
VariantAnnotation
updated 10.3 years ago by
Julian Gehring
★ 1.3k • written 10.3 years ago by
Marco Blanchette
▴ 220
2
votes
3
replies
5.5k
views
Linkage disequilibrium with 1000 Genomes/HapMap
HapMap
genomes
HapMap
genomes
10.4 years ago
enricoferrero
▴ 660
0
votes
3
replies
1.7k
views
Elephant shark genome
Biostrings
genomes
Biostrings
genomes
updated 10.7 years ago by
Martin Morgan
25k • written 10.7 years ago by
Guest User
★ 13k
0
votes
1
reply
2.2k
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 10.7 years ago by
Lukas Chavez
▴ 570 • written 10.7 years ago by
Vining, Kelly
▴ 220
0
votes
1
reply
1.7k
views
GOseq with ce6
GO
Yeast
Organism
goseq
genomes
GO
Yeast
Organism
goseq
genomes
updated 10.7 years ago by
Nadia Davidson
▴ 320 • written 10.7 years ago by
François Lefebvre
▴ 50
0
votes
0
replies
1.8k
views
Trying to use BSgenome.Hsapiens.NCBI.GRCh38
Cancer
BSgenome
BSgenome
genomes
Cancer
BSgenome
BSgenome
genomes
10.7 years ago
Hervé Pagès
16k
0
votes
1
reply
1.9k
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 10.7 years ago by
Lukas Chavez
▴ 570 • written 10.7 years ago by
Vining, Kelly
▴ 220
0
votes
5
replies
2.1k
views
Rsamtools filtering bam file: RE: MEDIPS.createSet error
GO
BSgenome
BSgenome
Rsamtools
genomes
MEDIPS
GO
BSgenome
BSgenome
Rsamtools
genomes
updated 10.7 years ago by
Martin Morgan
25k • written 10.7 years ago by
Vining, Kelly
▴ 220
0
votes
3
replies
2.3k
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
10.9 years ago
Guest User
★ 13k
0
votes
1
reply
1.8k
views
makeTranscriptDbFromUCSC() error
genomes
genomes
10.9 years ago
Chris Cabanski
▴ 30
0
votes
2
replies
2.4k
views
ensemblVEP, variant_effect_predictor versions and release schedule
Transcription
HapMap
PolyPhen
SIFT
convert
genomes
ensemblVEP
Transcription
HapMap
SIFT
updated 10.9 years ago by
Valerie Obenchain
★ 6.8k • written 11.0 years ago by
Thomas Sandmann
▴ 30
0
votes
1
reply
2.4k
views
Pairwise Alignment on Large Protein Sequence Data Set
Alignment
genomes
Alignment
genomes
updated 11.0 years ago by
Hervé Pagès
16k • written 11.0 years ago by
Guest User
★ 13k
0
votes
0
replies
1.6k
views
Gviz and Leishmania genomes
rtracklayer
genomes
Gviz
rtracklayer
genomes
Gviz
11.1 years ago
florian.hahne@novartis.com
★ 1.6k
0
votes
0
replies
2.0k
views
Create a sample file /tab delimited file in QuasR
BSgenome
convert
BSgenome
genomes
QuasR
BSgenome
convert
BSgenome
genomes
QuasR
11.1 years ago
Michael Stadler
▴ 350
0
votes
1
reply
1.8k
views
makeTranscriptDbFromGFF fails on NCBI Bacteria genomes
GO
TranscriptDb
goseq
genomes
GO
TranscriptDb
goseq
genomes
updated 11.2 years ago by
Marc Carlson
★ 7.2k • written 11.2 years ago by
刘鹏飞
▴ 80
0
votes
1
reply
1.7k
views
Lifting over a bam file with Rsamtools and GenomicRanges
GenomicRanges
genomes
GenomicRanges
genomes
updated 11.3 years ago by
Michael Lawrence
★ 11k • written 11.3 years ago by
Guest User
★ 13k
0
votes
0
replies
1.3k
views
SnpStats - STRING_ELT() error and Fst
genomes
genomes
11.3 years ago
Voke AO
▴ 760
0
votes
1
reply
1.4k
views
Working with non-type strain annotation
Proteomics
GO
genomes
Proteomics
GO
genomes
updated 11.6 years ago by
Marc Carlson
★ 7.2k • written 11.6 years ago by
Thomas Lin Pedersen
▴ 70
0
votes
8
replies
3.5k
views
QuasR: how to use an indexed reference genome?
BSgenome
BSgenome
genomes
QuasR
BSgenome
BSgenome
genomes
QuasR
updated 11.6 years ago by
Michael Stadler
▴ 350 • written 11.6 years ago by
Paul Shannon
▴ 750
0
votes
2
replies
1.8k
views
QuasR special case alignment
Alignment
genomes
QuasR
Alignment
genomes
QuasR
updated 11.6 years ago by
Ugo Borello
▴ 340 • written 11.6 years ago by
Michael Stadler
▴ 350
0
votes
6
replies
1.8k
views
coverage on very large ReadGappedAlignmentsObject
Coverage
genomes
Coverage
genomes
updated 11.6 years ago by
Martin Morgan
25k • written 11.6 years ago by
Stefanie
▴ 360
0
votes
1
reply
2.1k
views
Help needed! What wrong with VariantAnnotation and TCGA vcfs
VariantAnnotation
genomes
VariantAnnotation
VariantAnnotation
genomes
VariantAnnotation
updated 11.7 years ago by
Martin Morgan
25k • written 11.7 years ago by
ying chen
▴ 340
0
votes
0
replies
1.7k
views
Useful information about Ensembl release 71 mart databases
zebrafish
PolyPhen
SIFT
affy
genomes
zebrafish
PolyPhen
SIFT
affy
genomes
11.7 years ago
Thomas Maurel
▴ 800
0
votes
0
replies
1.6k
views
Biostatistician position in London
Cancer
genomes
Cancer
genomes
11.7 years ago
Kathi Zarnack
▴ 110
0
votes
2
replies
1.6k
views
Limit on number of sequence files for forging a BSgenome
GO
Cancer
BSgenome
BSgenome
genomes
GO
Cancer
BSgenome
BSgenome
genomes
11.7 years ago
Hervé Pagès
16k
50 results • Page
1 of 1
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Comment: Biostrings: Error writing long reads (>200 kbps) with writeQualityScaledXStringS
by
Aidan
▴ 60
Quick update: this is fixed in a branch awaiting PR to Biostrings (https://github.com/Bioconductor/Biostrings/pull/122). Should be in `deve…
Answer: Can DESeq2's design compensate for sequencing experimental design shortcomings?
by
Michael Love
43k
For statistical analysis plans, I recommend working with a local statistician or someone familiar with linear models in R. I have to reserv…
Comment: how should I apply "cpg.annotate" to TCGA methylation data in hg38 for HM450K?
by
xiaofeiwang198266
• 0
Thanks for your reply!
Comment: Issues with seqlevelsStyle when making custom txdb objects for genomes/annotatio
by
Hervé Pagès
16k
> I have requested gDNAx developers for a feature request to turn off seqlevelsStyle(txdb) Yes, that's the right course of action. `seqlev…
Comment: ISO a solution to rank-order introns by transcript
by
mat149
▴ 80
Hey, In revisiting this question, the following code works for the '+' strand. I am having issues with demarcating intron rank by transcri…
Votes
C: edgeR and lack of counts ID on CPM matrix
A: DESeq2 Following RSEM
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A: Expected counts from RSEM in DESeq2
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