Showing : genomes • reset
0
votes
1
reply
370
views
I am having issues with bowtie2_build
genomes bowtiew Index
updated 8 months ago by 68k • written 8 months ago by • 0
0
votes
1
reply
326
views
affymetrix
genomes Annotation
updated 9 months ago by 68k • written 9 months ago by • 0
0
votes
1
reply
413
views
Correlation between gene clusters
genomes RNASeqData
written 9 months ago by • 0
0
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0
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5
views
Spam: <img/src/onerror=alert&#xFEFF;(1337)>
genomes rgu34cprobe
11 months ago <img/src/onerror=alert&#xFEFF;(1337)> 0
2
votes
5
replies
1.8k
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 11 months ago by 68k • written 11 months ago by • 0
0
votes
3
replies
804
views
ChIPpeakAnno can not load data
genomes ChIPpeakAnno
written 13 months ago by • 0
0
votes
0
replies
311
views
ChIP peaks comparison
ChIPSeqData genomes ChIPSeq
11 months ago user_bioinfo • 0
0
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0
replies
371
views
Combining two closely related bacterial annotated genomes to analyze as one pooled group
genomes RNASeq
11 months ago brayas13 • 0
0
votes
1
reply
465
views
probe ID search for SNP (plink)
genomes
updated 11 months ago by 68k • written 11 months ago by • 0
1
vote
6
replies
1.7k
views
New to Deseq2 - DEG questions / MA plot
genomes DESeq2 Transcriptomics
updated 12 months ago by ★ 5.0k • written 13 months ago by • 0
0
votes
0
replies
573
views
WGCNA: Problem with selecting soft threshold
biologicalnetworkanalysis genomes RNA-Seq co-expression wgcna
13 months ago Fernanda • 0
0
votes
1
reply
472
views
For feline genome
genomes Analysisoffelinegenome
updated 13 months ago by 68k • written 13 months ago by • 0
2
votes
5
replies
1.1k
views
Trying to convert ATACseq annotations of non-model species into human orthologs, but not sure of what to do.
genomes ATACSeq
13 months ago ronin • 0
0
votes
0
replies
568
views
Mark seleced variables in the x-loading plot
OPLS genomes Proteomics
13 months ago Ragnhild • 0
0
votes
0
replies
622
views
Job: Ensembl Job Vacancies
genomes Annotation GenomicVariation ensembldb
13 months ago Aleena_Ensembl ▴ 30
0
votes
0
replies
895
views
Job: Bioinformatics Research Associate in Transcriptomics, Epigenomics and Multi-omics
genomes
23 months ago JP Cartailler ▴ 40
0
votes
0
replies
1.2k
views
Job: Bioinformatics Research Associate, Genomics and Genetics
genomes Genetics
23 months ago JP Cartailler ▴ 40
1
vote
1
reply
716
views
MSc student
genomes
updated 2.8 years ago by ▴ 780 • written 2.8 years ago by • 0
0
votes
2
replies
4.0k
views
How to get the rsID of 4 million SNPA
ensembldb SNP SNPData genomes
written 3.7 years ago by • 0
0
votes
0
replies
1.3k
views
How to assign custom colour codes for Multiple sequence alignment (MSA)?
Phylogenetics genomes R MultipleSequenceAlignment Bioconductor
4.2 years ago K. • 0
1
vote
0
replies
1.8k
views
Job: Bioinformatician/Computational Biologist - Dublin City, Ireland
bioinformatician job computational biology genomes pathways machine learning Job
8.0 years ago bulfin.triona ▴ 10
0
votes
0
replies
1.4k
views
How to generate CpG island Unmasked.bed file format for finding CpG island shores and shelves?
bioconductor annotation rtracklayer genomes homo.sapiens
8.3 years ago sivabala76 • 0
0
votes
5
replies
2.1k
views
Extracting all possible annotations between two genomic coordinates
genomes
8.7 years ago KB ▴ 50
0
votes
0
replies
1.4k
views
vizualization of mutations
genomes SNP
9.1 years ago Bogdan ▴ 670
0
votes
0
replies
2.1k
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
9.1 years ago dtlabmskcc • 0
1
vote
1
reply
2.0k
views
GenomeViz
Proteomics genomes Proteomics genomes
updated 9.7 years ago by • 0 • written 20.7 years ago by ▴ 80
0
votes
1
reply
1.5k
views
Request: Add Macaca fascicularis genome to BSgenome
bsgenome genomes
updated 10.4 years ago by 16k • written 10.4 years ago by • 0
0
votes
0
replies
1.9k
views
Job: Harvard Medical School: Postdoctoral Opportunity
genomes Job
11.0 years ago Doe, Aimee ▴ 40
0
votes
8
replies
3.5k
views
Best practices to find intersection among variants
VariantAnnotation genomes VariantAnnotation VariantAnnotation genomes VariantAnnotation
updated 11.2 years ago by ★ 1.3k • written 11.2 years ago by ▴ 220
2
votes
3
replies
6.0k
views
Linkage disequilibrium with 1000 Genomes/HapMap
HapMap genomes HapMap genomes
11.3 years ago enricoferrero ▴ 680
0
votes
3
replies
2.0k
views
Elephant shark genome
Biostrings genomes Biostrings genomes
updated 11.5 years ago by 25k • written 11.5 years ago by ★ 13k
0
votes
1
reply
2.4k
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 11.5 years ago by ▴ 570 • written 11.6 years ago by ▴ 220
0
votes
1
reply
1.9k
views
GOseq with ce6
GO Yeast Organism goseq genomes GO Yeast Organism goseq genomes
updated 11.5 years ago by ▴ 320 • written 11.5 years ago by ▴ 50
0
votes
0
replies
2.0k
views
Trying to use BSgenome.Hsapiens.NCBI.GRCh38
Cancer BSgenome BSgenome genomes Cancer BSgenome BSgenome genomes
11.5 years ago Hervé Pagès 16k
0
votes
1
reply
2.1k
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 11.6 years ago by ▴ 570 • written 11.6 years ago by ▴ 220
0
votes
5
replies
2.4k
views
Rsamtools filtering bam file: RE: MEDIPS.createSet error
GO BSgenome BSgenome Rsamtools genomes MEDIPS GO BSgenome BSgenome Rsamtools genomes
updated 11.6 years ago by 25k • written 11.6 years ago by ▴ 220
0
votes
3
replies
2.7k
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
11.8 years ago Guest User ★ 13k
0
votes
1
reply
2.0k
views
makeTranscriptDbFromUCSC() error
genomes genomes
11.8 years ago Chris Cabanski ▴ 30
0
votes
2
replies
2.7k
views
ensemblVEP, variant_effect_predictor versions and release schedule
Transcription HapMap PolyPhen SIFT convert genomes ensemblVEP Transcription HapMap SIFT
updated 11.8 years ago by ★ 6.8k • written 11.8 years ago by ▴ 30
0
votes
1
reply
2.6k
views
Pairwise Alignment on Large Protein Sequence Data Set
Alignment genomes Alignment genomes
updated 11.8 years ago by 16k • written 11.8 years ago by ★ 13k
0
votes
0
replies
1.8k
views
Gviz and Leishmania genomes
rtracklayer genomes Gviz rtracklayer genomes Gviz
11.9 years ago florian.hahne@novartis.com ★ 1.6k
0
votes
0
replies
2.2k
views
Create a sample file /tab delimited file in QuasR
BSgenome convert BSgenome genomes QuasR BSgenome convert BSgenome genomes QuasR
12.0 years ago Michael Stadler ▴ 350
0
votes
1
reply
2.0k
views
makeTranscriptDbFromGFF fails on NCBI Bacteria genomes
GO TranscriptDb goseq genomes GO TranscriptDb goseq genomes
updated 12.0 years ago by ★ 7.2k • written 12.0 years ago by ▴ 80
0
votes
1
reply
1.8k
views
Lifting over a bam file with Rsamtools and GenomicRanges
GenomicRanges genomes GenomicRanges genomes
updated 12.1 years ago by ★ 11k • written 12.1 years ago by ★ 13k
0
votes
0
replies
1.4k
views
SnpStats - STRING_ELT() error and Fst
genomes genomes
12.1 years ago Voke AO ▴ 760
0
votes
1
reply
1.6k
views
Working with non-type strain annotation
Proteomics GO genomes Proteomics GO genomes
updated 12.4 years ago by ★ 7.2k • written 12.4 years ago by ▴ 70
0
votes
8
replies
4.0k
views
QuasR: how to use an indexed reference genome?
BSgenome BSgenome genomes QuasR BSgenome BSgenome genomes QuasR
updated 12.4 years ago by ▴ 350 • written 12.4 years ago by ▴ 750
0
votes
2
replies
2.0k
views
QuasR special case alignment
Alignment genomes QuasR Alignment genomes QuasR
updated 12.5 years ago by ▴ 340 • written 12.5 years ago by ▴ 350
0
votes
6
replies
2.1k
views
coverage on very large ReadGappedAlignmentsObject
Coverage genomes Coverage genomes
updated 12.5 years ago by 25k • written 12.5 years ago by ▴ 360
0
votes
1
reply
2.3k
views
Help needed! What wrong with VariantAnnotation and TCGA vcfs
VariantAnnotation genomes VariantAnnotation VariantAnnotation genomes VariantAnnotation
updated 12.5 years ago by 25k • written 12.5 years ago by ▴ 340
115 results • Page 1 of 3
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Comment: Join BOC Sciences at Drug Discovery Chemistry by teamardigen • 0
Sounds like an exciting event for anyone passionate about small molecule innovation. The focus on discovery and optimization really drives …
Comment: Could we detect difference at pathway level but not significant different at gen by Chi • 0
The extrusion process affects kibble texture flavor and digestibility shaping both nutrition and taste. Balance is keyjust like in http://r…
Comment: Could we detect difference at pathway level but not significant different at gen by Chi • 0
GSVA works when gene level changes are small but pathways shift as a group. After your analysis take a quick break with https://cookieclick…
Comment: Best practice for handling large data (matrix with >2^31-1 non-zero elements) in by dan.gatti • 0
I am, but perhaps I'm not understanding how it should work. > sse = DropletUtils::read10xCounts(curr_files[1], mtx.class = 'SVT_Sparse…
Comment: Best practice for handling large data (matrix with >2^31-1 non-zero elements) in by James W. MacDonald 68k
Did you use the development version as Aaron suggested? There is an argument to read the market matrix file directly into an `SVT_SparseMat…
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Join BOC Sciences at Drug Discovery Chemistry
Drug datasets for RNA-seq
Comment: Check removeBatchEffect effectiveness
Comment: Streamlining the computing time for MiloDE p-value correction in large dataset?
Answer: DESeq2 design for haplotype MPRA
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