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Showing :
genomes
•
reset
0
votes
3
replies
389
views
ChIPpeakAnno can not load data
genomes
ChIPpeakAnno
written 9 weeks ago by
文杰
• 0
0
votes
0
replies
112
views
ChIP peaks comparison
ChIPSeqData
genomes
ChIPSeq
15 days ago
user_bioinfo
• 0
0
votes
0
replies
118
views
Combining two closely related bacterial annotated genomes to analyze as one pooled group
genomes
RNASeq
16 days ago
brayas13
• 0
0
votes
1
reply
248
views
probe ID search for SNP (plink)
genomes
updated 21 days ago by
James W. MacDonald
67k • written 22 days ago by
유빈
• 0
1
vote
6
replies
685
views
New to Deseq2 - DEG questions / MA plot
genomes
DESeq2
Transcriptomics
updated 4 weeks ago by
ATpoint
★ 4.5k • written 8 weeks ago by
Newbie
• 0
0
votes
0
replies
179
views
WGCNA: Problem with selecting soft threshold
biologicalnetworkanalysis
genomes
RNA-Seq
co-expression
wgcna
8 weeks ago
Fernanda
• 0
0
votes
1
reply
259
views
For feline genome
genomes
Analysisoffelinegenome
updated 8 weeks ago by
James W. MacDonald
67k • written 8 weeks ago by
Ritu
• 0
2
votes
5
replies
650
views
Trying to convert ATACseq annotations of non-model species into human orthologs, but not sure of what to do.
genomes
ATACSeq
9 weeks ago
ronin
• 0
0
votes
0
replies
245
views
Mark seleced variables in the x-loading plot
OPLS
genomes
Proteomics
9 weeks ago
Ragnhild
• 0
0
votes
0
replies
268
views
Job:
Ensembl Job Vacancies
genomes
Annotation
GenomicVariation
ensembldb
12 weeks ago
Aleena
▴ 30
0
votes
0
replies
600
views
Job:
Bioinformatics Research Associate in Transcriptomics, Epigenomics and Multi-omics
genomes
12 months ago
JP Carter
▴ 40
0
votes
0
replies
588
views
Job:
Bioinformatics Research Associate, Genomics and Genetics
genomes
Genetics
12 months ago
JP Carter
▴ 40
1
vote
1
reply
557
views
MSc student
genomes
updated 22 months ago by
Basti
▴ 780 • written 22 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 2.7 years ago by
Weiqiong
• 0
0
votes
0
replies
1.0k
views
How to assign custom colour codes for Multiple sequence alignment (MSA)?
Phylogenetics
genomes
R
MultipleSequenceAlignment
Bioconductor
3.3 years ago • updated 3.2 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
7.1 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
7.4 years ago
sivabala76
• 0
0
votes
5
replies
1.7k
views
Extracting all possible annotations between two genomic coordinates
genomes
7.8 years ago • updated 7.7 years ago
KB
▴ 50
0
votes
0
replies
1.2k
views
vizualization of mutations
genomes
SNP
8.2 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
8.2 years ago
dtlabmskcc
• 0
1
vote
1
reply
1.8k
views
GenomeViz
Proteomics
genomes
Proteomics
genomes
updated 8.8 years ago by
xianxiu
• 0 • written 19.8 years ago by
Rohit Ghai
▴ 80
0
votes
1
reply
1.3k
views
Request: Add Macaca fascicularis genome to BSgenome
bsgenome
genomes
updated 9.5 years ago by
Hervé Pagès
16k • written 9.5 years ago by
amy.klegarth
• 0
0
votes
0
replies
1.7k
views
Job:
Harvard Medical School: Postdoctoral Opportunity
genomes
Job
10.1 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 10.2 years ago by
Julian Gehring
★ 1.3k • written 10.2 years ago by
Marco Blanchette
▴ 220
2
votes
3
replies
5.4k
views
Linkage disequilibrium with 1000 Genomes/HapMap
HapMap
genomes
HapMap
genomes
10.3 years ago
enricoferrero
▴ 660
0
votes
3
replies
1.7k
views
Elephant shark genome
Biostrings
genomes
Biostrings
genomes
updated 10.6 years ago by
Martin Morgan
25k • written 10.6 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 10.6 years ago by
Lukas Chavez
▴ 570 • written 10.6 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 10.6 years ago by
Nadia Davidson
▴ 320 • written 10.6 years ago by
François Lefebvre
▴ 50
0
votes
0
replies
1.7k
views
Trying to use BSgenome.Hsapiens.NCBI.GRCh38
Cancer
BSgenome
BSgenome
genomes
Cancer
BSgenome
BSgenome
genomes
10.6 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 10.6 years ago by
Lukas Chavez
▴ 570 • written 10.6 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 10.6 years ago by
Martin Morgan
25k • written 10.6 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 10.9 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 10.9 years ago by
Hervé Pagès
16k • written 10.9 years ago by
Guest User
★ 13k
0
votes
0
replies
1.6k
views
Gviz and Leishmania genomes
rtracklayer
genomes
Gviz
rtracklayer
genomes
Gviz
11.0 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 11.1 years ago by
Marc Carlson
★ 7.2k • written 11.1 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 11.2 years ago by
Michael Lawrence
★ 11k • written 11.2 years ago by
Guest User
★ 13k
0
votes
0
replies
1.3k
views
SnpStats - STRING_ELT() error and Fst
genomes
genomes
11.2 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 11.5 years ago by
Marc Carlson
★ 7.2k • written 11.5 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 11.5 years ago by
Michael Stadler
▴ 350 • written 11.5 years ago by
Paul Shannon
▴ 750
0
votes
2
replies
1.8k
views
QuasR special case alignment
Alignment
genomes
QuasR
Alignment
genomes
QuasR
updated 11.5 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 11.5 years ago by
Martin Morgan
25k • written 11.5 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 11.6 years ago by
Martin Morgan
25k • written 11.6 years ago by
ying chen
▴ 340
0
votes
0
replies
1.6k
views
Useful information about Ensembl release 71 mart databases
zebrafish
PolyPhen
SIFT
affy
genomes
zebrafish
PolyPhen
SIFT
affy
genomes
11.6 years ago
Thomas Maurel
▴ 800
0
votes
0
replies
1.5k
views
Biostatistician position in London
Cancer
genomes
Cancer
genomes
11.6 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
11.6 years ago
Hervé Pagès
16k
3
votes
4
replies
1.4k
views
Limit on number of sequence files for forging a BSgenome
BSgenome
BSgenome
genomes
BSgenome
BSgenome
genomes
updated 11.7 years ago by
Kasper Daniel Hansen
★ 6.5k • written 11.7 years ago by
Marco Blanchette
▴ 220
0
votes
2
replies
1.1k
views
Expected value of finding a sequence (Tim Smith)
genomes
genomes
updated 11.7 years ago by
Alvaro J. González
▴ 10 • written 11.7 years ago by
Alvaro J. González
▴ 80
50 results • Page
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Answer: Unlocking Potential: NURS FPX Strategies and Insights
by
efsane_kral2000
• 0
https://diendannhansu.com/threads/hayal-sohbet-odalari.667004/ https://forum.realdigital.org/u/serkan https://animefagos.com/miembros/ser…
Comment: Unlocking Potential: NURS FPX Strategies and Insights
by
efsane_kral2000
• 0
https://www.hayalsohbet.net https://www.yerlichat.com https://www.yerlichat.net https://www.mavisim.net https://www.hayalchat.com http…
Comment: Is it recommended to analyze different tissues together when using edgeR
by
Gordon Smyth
51k
Just plot the samples with plotMDS(). Alternatively you would use `voomLmFit()` with `sample.weights=TRUE` or `var.group=tissue`. In princ…
Comment: Handling Epic Array Data
by
Melisa Tecik
• 0
Thanks a lot for the help. You saved my day
Answer: Differene between the Wald and LRT test for time-series gene expression data
by
James W. MacDonald
67k
The advantage to using the LRT is that it's an omnibus test that tells you if there are changes at any time point. If you have lots of time…
Votes
Answer: Using voom-transformed counts for unsupervised analyses (PCA, Random Forest, Ela
Answer: Allele frequencies for ALL alleles of one SNP ?
Answer: Is it recommended to analyze different tissues together when using edgeR
Answer: Is it recommended to analyze different tissues together when using edgeR
Answer: Using Affymetrix Custom Array
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67k
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