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288 results • Page
3 of 6
Sort: Votes
Rank
Views
Votes
Replies
2
votes
3
replies
293
views
Editing Human Reference Genome by adding a CDS
gff
agat
transcriptome
updated 6 days ago by
Michael
54k • written 6 days ago by
LDT
▴ 340
2
votes
3
replies
302
views
How to establish haplotype-specific gene expression levels
RNA-seq
Haplotype
updated 1 day ago by
dsull
★ 5.8k • written 14 days ago by
javanokendo
▴ 60
1
vote
9
replies
1.2k
views
Supergnova stuck in tutorial
Genetic
Correlations
Python
Supergnova
Conda
updated 5 days ago by
Murat
• 0 • written 19 months ago by
Gerard
▴ 10
1
vote
2
replies
1.4k
views
How to download a list pdb codes contained in a csv file using
Biopython
updated 6 days ago by
Ram
43k • written 3.1 years ago by
jmungar2
▴ 10
1
vote
2
replies
194
views
Interpretation of combined P values - RNA microarray meta analysis
metaanalysis
R
microarray
DExMA
combinedP
6 days ago by
hagl
▴ 10
1
vote
3
replies
288
views
Merging vcf files with bcftools ([E::get_intv] Failed to parse TBX_VCF, was wrong -p [type] used?)
vcf
tabix
bcftools
updated 6 days ago by
Pierre Lindenbaum
161k • written 12 days ago by
giulia.cosenza
• 0
1
vote
2
replies
328
views
Forum:
VCF bulk handling
bcftools
SnpEff
WGS
VEP
VCF
6 days ago by
Javier
• 0
1
vote
1
reply
218
views
Retrieve a % coverage for each transcript
RNA-seq
updated 6 days ago by
Ram
43k • written 6 days ago by
jammydodger123456
▴ 40
1
vote
2
replies
266
views
Can I readmap short reads to rDNA references?
rDNA
assembly
updated 6 days ago by
Ram
43k • written 6 days ago by
aniigodwinn
• 0
1
vote
4
replies
2.2k
views
Remove batch effect for prediction of RNA-seq data
RNA-Seq
batch-effect
Random-Forest
updated 6 days ago by
Ram
43k • written 4.7 years ago by
Vlad
▴ 10
1
vote
8
replies
3.4k
views
Best way to address different batches of RNA-seq
sequence
RNA-Seq
RPKM
Fold-Change
batch-effect
updated 6 days ago by
Ram
43k • written 7.0 years ago by
tud55122
▴ 20
1
vote
4
replies
2.4k
views
Batch effect control in GWAS data.
Batch-effect
omniexpress
GWAS
GSA
updated 6 days ago by
Ram
43k • written 4.8 years ago by
saksis.rihards
▴ 10
1
vote
1
reply
1.3k
views
Can we use previous estimated ComBat model to correct batch effects for new data?
microarray
RNA-Seq
batch-effect
updated 6 days ago by
Ram
43k • written 5.0 years ago by
Min Dai
▴ 160
1
vote
4
replies
2.8k
views
removing confounding batch effect with RUVseq
RUVseq
RNA-Seq
batch-effect
DESeq2
updated 6 days ago by
Ram
43k • written 5.1 years ago by
grant.hovhannisyan
★ 2.6k
1
vote
2
replies
2.1k
views
RNA-seq unbalanced batch effect correction
RNA-Seq
edgeR
R
Batch-Effect
updated 6 days ago by
Ram
43k • written 5.6 years ago by
sckinta
▴ 730
1
vote
1
reply
267
views
Inconsistency in SNP detection pipelines for multi-sample analysis
vcf
bam
bcf
snps
updated 6 days ago by
LChart
3.9k • written 6 days ago by
George
▴ 10
1
vote
0
replies
168
views
Tutorial:
DNA Methylation: Sequencing Techniques
WGBS
RRBS
5 days ago by
Novogene
▴ 420
1
vote
4
replies
674
views
What happened to Tombo Re-squiggle
Tombo
resquiggle
ONT
updated 5 days ago by
Ram
43k • written 3 months ago by
turcoa1
• 0
1
vote
1
reply
364
views
Problem with Mirdeep2 and Randfold output
mirdeep2
Randfold
5 days ago by
otieno43
▴ 30
1
vote
2
replies
1.9k
views
Remove batch effect from exome data
NGS
exome-sequencing
batch-effect
updated 5 days ago by
Ram
43k • written 6.5 years ago by
Alternative
▴ 270
1
vote
2
replies
2.9k
views
Taking surrogate variable into account before running PCA
sva
svaseq
batch-effect
updated 5 days ago by
Ram
43k • written 6.9 years ago by
wamiqsaifi
• 0
1
vote
3
replies
2.0k
views
gene expression data analysis and batch effect methods
microarray
Gene-expression
batch-effect
updated 5 days ago by
Ram
43k • written 6.9 years ago by
Shamim Sarhadi
▴ 220
1
vote
4
replies
3.1k
views
remove batch effect for multiple tumor data
RNA-Seq
batch-effect
updated 5 days ago by
Ram
43k • written 7.1 years ago by
hellocita
▴ 40
1
vote
4
replies
1.4k
views
Removing/Accounting for batch effects in unbalanced group RNAseq data
rna-seq
batch-effect
deseq
updated 5 days ago by
Ram
43k • written 2.2 years ago by
claysandel
• 0
1
vote
0
replies
2.1k
views
Tool:
DASC -- detecting hidden batch effects in gene expression datasets (Array/RNA-Seq/scRNA-Seq)
RNA-Seq
scRNA-Seq
R
Batch-Effect
updated 5 days ago by
Ram
43k • written 6.9 years ago by
Ar
★ 1.1k
1
vote
3
replies
3.3k
views
How to correct for batch effect in microarray meta-analysis
ComBat
microarray
meta-analysis
batch-effect
updated 5 days ago by
Ram
43k • written 9.9 years ago by
BrunoGiotti
▴ 120
1
vote
3
replies
3.6k
views
Does Harmony batch correction for scRNA-seq require the same populations to be present in all samples?
Harmony
single-cell
scRNA-seq
batch-effect
updated 5 days ago by
Ram
43k • written 4.5 years ago by
Lucy
▴ 140
1
vote
4
replies
1.7k
views
Batch correction and DE analysis of miRNA Seq data
miRNAseq
Differential-Expression
batch-effect
updated 5 days ago by
Ram
43k • written 5.1 years ago by
georgians
▴ 50
1
vote
4
replies
13k
views
RNA sequencing data batch effect removal
RNA-Seq
batch-effect
updated 5 days ago by
Ram
43k • written 7.4 years ago by
Tenghui Chen
• 0
1
vote
3
replies
4.1k
views
Evaluating removing batch effect tools with PCA or MDS?
bioconductor
limma
sva
r
batch-effect
updated 5 days ago by
Ram
43k • written 7.6 years ago by
Lluís R.
★ 1.2k
1
vote
1
reply
406
views
Plink merge errors.
cygwin64
bed
PLINK
4 days ago by
Dinmukhamed
• 0
1
vote
5
replies
683
views
RNA seq differential expression analysis
RNA-seq
normalization
updated 4 days ago by
BioinfGuru
★ 1.7k • written 5 days ago by
rrehimi
• 0
1
vote
1
reply
378
views
Load a full GFF3 into annotation track using arrow (Apollo)
arrow
python-apollo
Apollo
4 days ago by
renan.igor
• 0
1
vote
5
replies
540
views
Duplicate marking, read names, and the SRA
SRA
MarkDuplicates
updated 4 days ago by
GenoMax
141k • written 4 days ago by
Luka
• 0
1
vote
1
reply
287
views
GTF file from Stringtie to R Studio for either Ballgown or DESeq2
Stringtie
Cufflinks
Ballgown
DESeq2
updated 4 days ago by
Ram
43k • written 4 days ago by
Nina
• 0
1
vote
0
replies
532
views
The majority of the sequences in Trinity ID do not start from start codons. Can the sequences still be used for primer design and validation?
Primers
TRINITY
3 days ago by
mathavanbioinfo
▴ 90
1
vote
1
reply
248
views
Removing Illumina microarray probes with no expression HumanHT-12v4
microarray
HumanHT-12v4
Illumina
updated 3 days ago by
Gordon Smyth
★ 7.0k • written 4 days ago by
Bioinformatician
• 0
1
vote
1
reply
405
views
Difference when using difference number of pathways score to compare between 3 groups
GSVA
Limma
updated 3 days ago by
Gordon Smyth
★ 7.0k • written 5 days ago by
Chris
▴ 260
1
vote
2
replies
223
views
permutation test in edgeR
rna-seq
edgeR
updated 1 day ago by
Gordon Smyth
★ 7.0k • written 15 days ago by
Netanel
• 0
1
vote
5
replies
223
views
Downsampling fastq file
downsample
fastq
updated 1 day ago by
Ram
43k • written 1 day ago by
marco.barr
▴ 80
1
vote
3
replies
2.4k
views
Problem to remove subset of patients with plink
plink
PED
updated 1 day ago by
chrchang523
10k • written 6.1 years ago by
Ginevra
▴ 10
1
vote
1
reply
126
views
WGCNA preservation analysis
WGCNA
preservation
updated 19 hours ago by
Michael
54k • written 20 hours ago by
michael.flower.14
▴ 180
1
vote
3
replies
164
views
Filter BAM to keep only alignments at an interval, ignoring reads spliced over
samtools
bam
splicing
18 hours ago by
WouterDeCoster
47k
1
vote
1
reply
132
views
Failed kmer content
kmer
illumina
ngs
updated 14 hours ago by
Ram
43k • written 22 hours ago by
Kasturi
• 0
1
vote
5
replies
279
views
DYH17 Structure Prediction
BLAST
Protein-Structure-Prediction
14 hours ago by
anasjamshed
▴ 120
1
vote
5
replies
578
views
Cell barcode whitelists for DNBelab C Series High-throughput Single-cell RNA Series Library Preparation Set?
cell-barcode
MGI
DNBelab
single-cell
updated 11 hours ago by
atowns21
• 0 • written 3 months ago by
benjamin.pyenson
• 0
1
vote
1
reply
83
views
Including plasmid in transcriptome assemblies
Bacteria
BOWTIE2
Transcriptomics
STAR
updated 9 hours ago by
GenoMax
141k • written 9 hours ago by
heelpPlease
• 0
1
vote
1
reply
89
views
Herald:
The Biostar Herald for Tuesday, April 23, 2024
herald
updated 8 hours ago by
Pierre Lindenbaum
161k • written 9 hours ago by
Biostar
2.7k
1
vote
4
replies
361
views
GTF file for Rhinolophus sinicus
Rhinolophus-sinicus
GTF
updated 1 hour ago by
atowns21
• 0 • written 5 months ago by
ara
• 0
1
vote
2
replies
72
views
HaplotypeCaller - only SNPs
HaplotypeCaller
GATK
updated 1 hour ago by
analyst
▴ 20 • written 6 hours ago by
lorena9132
• 0
288 results • Page
3 of 6
Recent Votes
Comment: Per base sequence content error in RNAseq analysis
Answer: Gene set enrichment analysis differences between 2020 and 2024
Answer: Gene set enrichment analysis differences between 2020 and 2024
Answer: Gene set enrichment analysis differences between 2020 and 2024
Comment: What is the real meaning of relative enrichment/peak height of ChIP-seq tracks?
Comment: TCGA2STAT Error: Firehose connection
Answer: HaplotypeCaller - only SNPs
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Comment: How to compare the quality of assemblies
by
kirillkirilenko
▴ 40
A haploid assembly is our goal. For purging we used prefix.p_ctg.gfa (assembly graph of primary contigs).
Comment: Is it Acceptable to Have Uniform Quality Scores in a FASTQ File?
by
Istvan Albert
100k
What I mean is that no sequencing run can be calibrated with the claimed precision. Where it could correctly distinguish between basecalls …
Comment: HaplotypeCaller - only SNPs
by
analyst
▴ 20
After HaplotypeCaller, you can use gatk SelectVariants to extract snps or indels from vcf file ([link to command][1]) [1]: https://gatk…
Comment: GTF file for Rhinolophus sinicus
by
atowns21
• 0
Ah gotcha. I guess what doesn't make sense to me is why a [paper][1] published in 2022 uses that reference genome. [1]: https://www.na…
Answer: Wilcox test using data slot (log normalized count values) of scRNA-seq between t
by
yxwucq
• 0
The best way is to generate a pseudo-bulk aggregation then apply edgeR or DESeq2. You can also directly use wilcoxon on sc-level, since man…
Comment: How to solve this RoseTTAFold colaboratory error?
by
Mensur Dlakic
★ 27k
There is a dedicated Discord group that deals with everything related to ColabFold and its derivatives. Below is an invitation to join that…
Comment: How do I use the STARSolo aligner with MGI DNBelab C series HT scRNAseq librarie
by
atowns21
• 0
Hmm, okay I'm not sure what is going on, but here is what I did: 1. Downloaded a single fastq: `parallel-fastq-dump --tmpdir . --threads …
Comment: What is the real meaning of relative enrichment/peak height of ChIP-seq tracks?
by
HyperEvo
• 0
Ok, thank you so much~
Comment: GTF file for Rhinolophus sinicus
by
GenoMax
141k
I was able to get the GTF file. I tried the fasta genome and it seemed to work but I did not complete the download. If you choose to ignore…
Comment: some error in building kraken2 database
by
Art1ess
• 0
I have 2 files output, no error logs... the .kreport file: 100.00 160136511 160136511 U 0 unclassified head .res…
Comment: TCGA2STAT Error: Firehose connection
by
LauferVA
4.2k
agree. from a data-centric (rather than software centric) standpoint, it shouldn't be hard to get the TCGA data you are looking for from o…
Comment: Redirection of Duplicate PMIDs
by
LauferVA
4.2k
yep. in this case id definitely start with the grant numbers themselves as others have indicated. i did not recommend this before due to un…
Comment: GTF file for Rhinolophus sinicus
by
atowns21
• 0
This download doesn't seem to work for me. There is a message on the website saying "Warning: contaminated. Status: RefSeq GCF_001888835.1 …
Answer: HaplotypeCaller - only SNPs
by
Pierre Lindenbaum
161k
Filter the vcf dowstream after haplotypecaller using bcftools or gatk variantfiltration
Answer: Gene set enrichment analysis differences between 2020 and 2024
by
geneontologyhelp
▴ 380
We have releases about monthly in order to keep our data accurate and reflect current understanding. In 4 years, there have been about 40 r…
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