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Sequencing
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2.0k
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Job:
Bioinformatics Scientist, Astex Pharmaceuticals
bioinformatician job
oncology
sequencing
drug development
Job
10.4 years ago
Harpreet Saini
▴ 30
1
vote
0
replies
1.6k
views
Genome editing analysis with Illumina sequencing
indel
sequencing
alignment
10.5 years ago
Merienne Nicolas
▴ 120
0
votes
0
replies
1.3k
views
Invitation Research Collaborations
cancer
microarray
mirna
sequencing
10.5 years ago
alexandru.floares
• 0
0
votes
0
replies
1.9k
views
Job:
Research Associate, Cambridge, UK - Oesophageal Cancer ICGC project
job
sequencing
methylation
expression
Job
10.7 years ago
Andy Lynch
▴ 120
3
votes
3
replies
4.6k
views
Clarrification of ReadDNAStringSet
sequencing
10.8 years ago
khouloud.madbouh
• 0
6
votes
1
reply
3.4k
views
[ReportingTools] HTMLReport of DESeq2 results using Ensembl Gene Ids
Sequencing
Annotation
convert
biomaRt
ReportingTools
DESeq2
Sequencing
Annotation
convert
updated 10.8 years ago by
andrew.j.skelton73
▴ 370 • written 11.9 years ago by
Jason Hackney
▴ 160
0
votes
0
replies
1.6k
views
Job:
Computational Biologist Research Associate Position at the University of Cambridge
cancer
sequencing
prostate
Job
11.0 years ago
Andy Lynch
▴ 120
0
votes
3
replies
1.2k
views
How does shearwater determine the reference sequence?
sequencing
11.1 years ago • updated 11.0 years ago
Asma rabe
▴ 290
0
votes
1
reply
6.8k
views
Missing SAM header?
sequencing
updated 11.0 years ago by
James W. MacDonald
68k • written 11.0 years ago by
Chris Fenton
▴ 80
0
votes
9
replies
3.1k
views
MEDIPS: how does MEDIPS define a methylated region / cluster?
Sequencing
MEDIPS
updated 11.1 years ago by
mengru1223
• 0 • written 11.1 years ago by
Guest User
★ 13k
0
votes
3
replies
1.6k
views
VariantTools, Shearwater and reference genome
sequencing
updated 11.1 years ago by
James W. MacDonald
68k • written 11.1 years ago by
Asma rabe
▴ 290
0
votes
4
replies
2.0k
views
segfault for pairwiseAlignment
sequencing
software error
alignment
updated 11.1 years ago by
Kasper Daniel Hansen
★ 6.5k • written 11.1 years ago by
Taub, Margaret
▴ 10
1
vote
0
replies
1.7k
views
Job:
PI position at EMBL-EBI (Cambridge UK)
Job
Sequencing
11.1 years ago
Wolfgang Huber
★ 13k
2
votes
0
replies
2.6k
views
Job:
Job Opening: Computational Biologist @ Genentech Bioinformatics
Job
Sequencing
Genetics
Cancer
updated 11.1 years ago by
Dan Tenenbaum
★ 8.2k • written 11.1 years ago by
Michael Lawrence
★ 11k
1
vote
2
replies
3.4k
views
Interaction categorical/continuous variable DESeq2
Sequencing
DESeq2
updated 11.1 years ago by
Wolfgang Huber
★ 13k • written 11.1 years ago by
Hugo Varet
▴ 80
0
votes
0
replies
2.5k
views
Rsubread featureCounts unexpected strand-specifc counts with Ensembl GTF
Sequencing
Annotation
11.1 years ago
Wei Shi
★ 3.6k
0
votes
3
replies
1.8k
views
edgeR: mixing technical replicates from Illumina HiSeq and MiSeq
Sequencing
Alignment
GO
edgeR
DESeq2
updated 11.1 years ago by
Ryan C. Thompson
★ 7.9k • written 11.1 years ago by
Nick N
▴ 60
0
votes
0
replies
1.5k
views
edgeR: mixing technical replicates from Illumina HiSeq and MiSeq
Sequencing
Alignment
GO
edgeR
DESeq2
Sequencing
Alignment
GO
edgeR
DESeq2
11.1 years ago
Gordon Smyth
53k
0
votes
1
reply
1.3k
views
edgeR: mixing technical replicates from Illumina HiSeq and MiSeq
Sequencing
edgeR
DESeq2
Sequencing
edgeR
DESeq2
updated 11.2 years ago by
Ryan C. Thompson
★ 7.9k • written 11.2 years ago by
Nicolas Delhomme
▴ 320
0
votes
3
replies
2.1k
views
edgeR: mixing technical replicates from Illumina HiSeq and MiSeq
Sequencing
Sequencing
updated 11.2 years ago by
Ryan C. Thompson
★ 7.9k • written 11.2 years ago by
Nick N
▴ 60
2
votes
5
replies
2.1k
views
DEXSeq update results change
Sequencing
DESeq
DEXSeq
Sequencing
DESeq
DEXSeq
11.2 years ago
António Miguel de Jesus Domingues
▴ 510
0
votes
3
replies
2.0k
views
finding differential expression pattern between paired columns of data frame.
Sequencing
SmallRNA
Microarray
limma
Sequencing
SmallRNA
Microarray
limma
updated 11.2 years ago by
James W. MacDonald
68k • written 11.2 years ago by
Jakub Stanislaw Nowak
▴ 70
0
votes
1
reply
2.3k
views
edgeR: Analyze mini-time-series MeDIP data of pooled DNAs without replicates?
Sequencing
edgeR
MEDIPS
Sequencing
edgeR
MEDIPS
11.2 years ago
Vang Le
▴ 80
0
votes
1
reply
1.2k
views
Designing a model with blocking and other interactions
Sequencing
Sequencing
updated 11.3 years ago by
Gordon Smyth
53k • written 11.3 years ago by
Eleanor Su
▴ 110
0
votes
1
reply
1.6k
views
DESeqs two-factor two-level, interaction is interested
Sequencing
GO
phyloseq
DESeq2
Sequencing
GO
phyloseq
DESeq2
11.3 years ago
Shucong Li
▴ 60
1
vote
2
replies
2.4k
views
DESeqs two-factor two-level, interaction is interested
Sequencing
GO
phyloseq
DESeq2
Sequencing
GO
phyloseq
DESeq2
updated 11.3 years ago by
Michael Love
43k • written 11.3 years ago by
Shucong Li
▴ 60
0
votes
0
replies
4.6k
views
cpm cutoff (edgeR) [was: total count filter cutoff (edgeR)]
Sequencing
miRNA
edgeR
Sequencing
miRNA
edgeR
11.3 years ago
Gordon Smyth
53k
0
votes
0
replies
1.1k
views
Practical Workshop on High-Throughput Sequencing Data Analysis. 6-10 Oct 2014, OIST, Okinawa, Japan
Sequencing
Sequencing
11.4 years ago
Gabriella Rustici
▴ 60
0
votes
0
replies
1.3k
views
ECCB 2014
Sequencing
Pathways
Sequencing
Pathways
11.4 years ago
Wolfgang Raffelsberger
▴ 60
0
votes
2
replies
3.3k
views
DE analysis with reference transcriptome
Sequencing
GO
Organism
edgeR
DESeq
EBSeq
Sequencing
GO
Organism
edgeR
DESeq
EBSeq
updated 11.4 years ago by
James W. MacDonald
68k • written 11.4 years ago by
Nicole Ertl
▴ 10
0
votes
1
reply
4.2k
views
ChIPseeker: Error in annotatePeak
Sequencing
GO
annotate
ChIPseeker
Sequencing
GO
annotate
ChIPseeker
11.5 years ago
António Miguel de Jesus Domingues
▴ 510
0
votes
0
replies
1.9k
views
Job: Bioinformatics Analyst at Johns Hopkins Medical School (Masters or Ph.D.)
Sequencing
Epigenetics
PROcess
Sequencing
Epigenetics
PROcess
11.5 years ago
Brian Herb
▴ 80
0
votes
0
replies
4.5k
views
Bioconductor 2.14 is released
BiocViews
aCGH
SNP
Sequencing
RNASeq
ChIPSeq
miRNA
Microarray
qPCR
Metabolomics
Coverage
11.5 years ago
Dan Tenenbaum
★ 8.2k
0
votes
1
reply
1.3k
views
CNV detection using cn.farms for non-affymetrix arrays (custom oligonucleotide arrays)
Sequencing
Microarray
probe
cn.mops
Sequencing
Microarray
probe
cn.mops
updated 11.5 years ago by
Djork Clevert
▴ 210 • written 11.5 years ago by
Guest User
★ 13k
0
votes
0
replies
1.0k
views
Announcement: (Free) Course 29-30 May, HPC Wales: Parallel Computing with R using SPRINT on post-genomic data
Sequencing
Sequencing
11.5 years ago
SPRINT
▴ 20
0
votes
8
replies
2.1k
views
Designing a model with blocking and other interactions
Sequencing
Sequencing
updated 11.6 years ago by
Gordon Smyth
53k • written 11.6 years ago by
Eleanor Su
▴ 110
0
votes
0
replies
744
views
Join expression values of replicas in edgeR
Sequencing
RNASeq
edgeR
Sequencing
RNASeq
edgeR
11.6 years ago
Gordon Smyth
53k
0
votes
0
replies
1.4k
views
Statistical Bioinformatician/Geneticist in Oxford
Sequencing
Genetics
Sequencing
Genetics
11.6 years ago
Steve Taylor
▴ 280
0
votes
0
replies
1.3k
views
CSAMA 2014: Computational Statistics for Genome Biology - June 22-27, 2014
Sequencing
Annotation
Classification
Clustering
Sequencing
Annotation
Classification
11.6 years ago
Wolfgang Huber
★ 13k
0
votes
0
replies
1.7k
views
Student Internships at Illumina Cambridge Ltd, UK
Sequencing
BaseSpaceR
Sequencing
BaseSpaceR
11.7 years ago
Adrian Alexa
▴ 400
0
votes
8
replies
3.0k
views
DEXSeq - too many exons in gene
Sequencing
Annotation
DEXSeq
Sequencing
Annotation
DEXSeq
updated 11.7 years ago by
Steve Lianoglou
★ 13k • written 11.7 years ago by
António Miguel de Jesus Domingues
▴ 510
0
votes
3
replies
1.2k
views
(EdgeR) statistical justification of partitioning dataset for multiple analysis
Sequencing
edgeR
Sequencing
edgeR
updated 11.7 years ago by
Ryan C. Thompson
★ 7.9k • written 11.7 years ago by
Adriaan Sticker
▴ 90
0
votes
7
replies
3.4k
views
[ReportingTools] and DESeq2 results, publish DESeqDataSet using resultsNames other than the default
Sequencing
ReportingTools
DESeq2
Sequencing
ReportingTools
DESeq2
updated 11.8 years ago by
James W. MacDonald
68k • written 11.8 years ago by
Dimitra Alexopoulou
▴ 30
0
votes
4
replies
1.6k
views
finding a very large number of false positives using edgeR
Sequencing
RNASeq
edgeR
Sequencing
RNASeq
edgeR
updated 11.8 years ago by
Gordon Smyth
53k • written 11.8 years ago by
Blum, Charles
▴ 20
0
votes
0
replies
1.5k
views
Job opening: Staff Scientist – Computational Biology and Bioinformatics – Massachusetts General Hospital, Boston, MA, USA
Sequencing
Microarray
Cancer
Sequencing
Microarray
Cancer
11.8 years ago
Wittner, Ben
▴ 290
0
votes
0
replies
1.9k
views
Job: Postdoc positions - Computational Biology - Center for Genomic Science, Milan, Italy
Sequencing
Cancer
Sequencing
Cancer
11.9 years ago
mattia pelizzola
▴ 200
5
votes
2
replies
3.5k
views
Gviz - show plus and minus strand from a bam
Sequencing
Coverage
Gviz
Sequencing
Coverage
Gviz
updated 11.9 years ago by
florian.hahne@novartis.com
★ 1.6k • written 11.9 years ago by
António Miguel de Jesus Domingues
▴ 510
0
votes
0
replies
1.4k
views
Job in statistical genetics / bioinformatics
Sequencing
Genetics
Sequencing
Genetics
11.9 years ago
Paul Leo
▴ 970
0
votes
2
replies
7.2k
views
how to obtain base counts from BAM file at specific genomic coordinates
SNP
Sequencing
Coverage
Alignment
Cancer
Biostrings
PROcess
IRanges
GenomicRanges
SNP
updated 12.0 years ago by
Michael Lawrence
★ 11k • written 12.0 years ago by
Hervé Pagès
16k
0
votes
0
replies
4.6k
views
Bioconductor 2.13 is released
BiocViews
aCGH
SNP
Transcription
Sequencing
miRNA
Microarray
Genetics
Proteomics
Coverage
12.0 years ago
Dan Tenenbaum
★ 8.2k
308 results • Page
2 of 7
Recent ...
Replies
Comment: Best practice for handling large data (matrix with >2^31-1 non-zero elements) in
by
James W. MacDonald
68k
Oh. ``` > z <- read10xCounts(c(tmpdir, tmpdir), mtx.class = "SVT_SparseMatrix", delayed = TRUE) > class(counts(z)) [1] "DelayedMatrix" att…
Comment: Best practice for handling large data (matrix with >2^31-1 non-zero elements) in
by
James W. MacDonald
68k
That's weird. Using the example data works for me. ``` > example(read10xCounts) rd10xC> # Mocking up some 10X genomics output. rd10xC> ex…
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: 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…
Votes
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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