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420 results • Page
3 of 9
Sort: replies
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Views
Votes
Replies
0
votes
3
replies
1.8k
views
How to remove batch effect in copy number segment mean
Combat
CNA
Batch-Effect
updated 22 days ago by
Ram
43k • written 5.5 years ago by
sugus
▴ 150
3
votes
3
replies
233
views
Gene Specific coverage from WGS data
linux
WGS
Bioinformatics
SARS
CoV2
3 days ago by
Adyasha
• 0
0
votes
2
replies
300
views
RNAseq 1 control 2 different treatment
RNA-seq
24 days ago by
matteo.levorato
• 0
0
votes
2
replies
172
views
Longitudinal analysis of subpopulations: which approach is better?
differential-expression
DEG
model
11 days ago by
Lluís R.
★ 1.2k
0
votes
2
replies
192
views
Correlating Bulk Differential Expression with quantitative
Differential-Expression
DESeq2
2 days ago by
Nicholas
• 0
0
votes
2
replies
290
views
Bedmethyl file format
bedmethyl
methylation
updated 23 days ago by
GenoMax
142k • written 23 days ago by
njornet
▴ 20
0
votes
2
replies
102
views
LncRNA Nomenclature
ENST
nomenclature
lncrna
GBB
ENSG
10 hours ago by
jain72744
▴ 10
0
votes
2
replies
1.0k
views
proportional hazard assumption was not satisfied for a covariate
hazard-ratios
Cox-model
survival
updated 23 days ago by
Ram
43k • written 4.4 years ago by
akutasame
▴ 40
0
votes
2
replies
254
views
Downloading older version of a tool
Alignment
tools
6 days ago by
Ruqaiya
• 0
2
votes
2
replies
221
views
Raw counts using stringtie
stringtie
RNA-seq
updated 7 days ago by
GenoMax
142k • written 7 days ago by
ahmad.sajad4541
• 0
1
vote
2
replies
347
views
Extracting information from gff3 file produced by augustus
augustus
gff3
updated 24 days ago by
Istvan Albert
100k • written 26 days ago by
Jiang
• 0
0
votes
2
replies
574
views
autodockvina
python
python3
autodock
updated 21 days ago by
Ram
43k • written 4 months ago by
iamsmor
• 0
1
vote
2
replies
269
views
permutation test in edgeR
rna-seq
edgeR
updated 18 days ago by
Gordon Smyth
★ 7.1k • written 4 weeks ago by
Netanel
• 0
0
votes
2
replies
418
views
How can I solve this error?
metal
22 days ago by
22211020193
• 0
1
vote
2
replies
243
views
Downloading full alignments from Pfam
pfam
5 days ago by
bef1
• 0
1
vote
2
replies
248
views
convert a seurat object to expressionset
Seurat
29 days ago by
Bine
▴ 60
0
votes
2
replies
293
views
VCF annotation with gnomADv4 using R package
annotation
gnomADv4
R
VCF
23 days ago by
DKA
▴ 40
2
votes
2
replies
2.6k
views
Pindel Segmentation Fault Error
pindel
updated 6 days ago by
Ruqaiya
• 0 • written 10.2 years ago by
Yuelin
▴ 20
2
votes
2
replies
215
views
PDB related issue
rcsb
pdb
updated 11 days ago by
noodle
▴ 580 • written 11 days ago by
Nafi
• 0
0
votes
2
replies
139
views
Presence of unknown sites in ANNOVAR output file
ANNOVAR
updated 1 day ago by
GenoMax
142k • written 1 day ago by
sainavyav22
• 0
0
votes
2
replies
311
views
bam merging for archaic samples
samtools
bam
updated 19 days ago by
Ram
43k • written 20 days ago by
Matteo Ungaro
▴ 100
1
vote
2
replies
304
views
Minimum RAM and Storage requirement for creating PSSM using ncbi-blast-2.2.30+-x64-linux
blast
pssm
9 days ago by
Nafi
• 0
0
votes
2
replies
244
views
How to detect and visualize ORFs in bacterial genome?
statistics
visualization
ORFs
genome
28 days ago by
marongiu.luigi
▴ 710
0
votes
2
replies
288
views
Calculating percentage of cells proliferating in single cell rna seq data
statistics
scRNA-seq
proliferation
23 days ago by
mropri
▴ 150
0
votes
2
replies
411
views
error in coding potential calculator CPC2
cpc
CPC2
coding-potential
21 days ago by
Ashok
• 0
5
votes
2
replies
1.8k
views
Batch effects from sequencing samples accross multiple flow cells.
rna-seq
batch
batch-effect
sequencing
updated 23 days ago by
Ram
43k • written 3.0 years ago by
Mat
▴ 60
0
votes
2
replies
161
views
Phasing a mixture of two individuals' DNA with long reads
long-reads
phasing
2 days ago by
njornet
▴ 20
0
votes
2
replies
461
views
QC exclusion of A/T or G/C alleles to avoid strand issues
quality-control
SNV
QC
SNP
21 days ago by
_quantum_girl_
▴ 10
0
votes
2
replies
456
views
miRNAs quantification using mirdeep2 tool
differential-expression
mirdeep2
miRNA
21 days ago by
Ashok
• 0
0
votes
2
replies
295
views
Abundance Calculation in MetaPhlAn 3: Methodology, TPM or RPKM, and the Treatment of Unclassified Reads
MetaPhlAn
Normalization
RPKM
TPM
27 days ago by
ramin.k2013
• 0
0
votes
2
replies
236
views
RNA editing sites based on DNA seq and RNA seq
RNA-editing
3 days ago by
Ahiad Chen Zion
• 0
0
votes
2
replies
292
views
WGCNA
PCA
WGCNA
EIGENGENE
28 days ago by
rajasekargutha
▴ 60
0
votes
2
replies
358
views
GSEA analysis in R
GSEA
R
Arabidopsis
22 days ago by
Sudip
• 0
0
votes
2
replies
296
views
Annovar using R package
Annovar
gnomAD
R
14 days ago by
DKA
▴ 40
1
vote
2
replies
272
views
alignment result
RNA-seq
samtools
hisat2
15 days ago by
ahmad.sajad4541
• 0
1
vote
2
replies
232
views
Need help for downloading arabdopsis thaliana reference genome fasta file and gtf file
Arabidopsis-thaliana
gtf
reference-genome
updated 10 days ago by
Ram
43k • written 10 days ago by
Ravita
• 0
0
votes
2
replies
326
views
Merging Outputs from plink --assoc and --hardy to Produce Table
PLINK
PANDAS
R
23 days ago by
Koketso
• 0
2
votes
2
replies
640
views
Batch correction for DE analysis
batch-correction
mRNA
RNA-seq
DEGs
MDSplot
updated 23 days ago by
Ram
43k • written 2.7 years ago by
Yoonji
▴ 10
2
votes
2
replies
324
views
How to calculate identity percentage between proteins contained in a FASTA file?
protein
FASTA
alignment
updated 15 days ago by
Ram
43k • written 16 days ago by
v.berriosfarias
▴ 140
1
vote
2
replies
268
views
POSSUM not working due to incompatible pssm file
fasta
pse-pssm
pssm
POSSUM
8 days ago by
rianna.collins
• 0
0
votes
2
replies
203
views
Differentail gene expression results
differential
expression
gene
rna-seq
Deseq2
updated 2 days ago by
swbarnes2
14k • written 3 days ago by
ahmad.sajad4541
• 0
1
vote
2
replies
315
views
Can I readmap short reads to rDNA references?
rDNA
assembly
updated 23 days ago by
Ram
43k • written 23 days ago by
aniigodwinn
• 0
0
votes
2
replies
208
views
Base Quality Score Recalibration with different reference genome
SNPs
GATK
BQSR
RNA-seq
7 days ago by
dtnondorf
• 0
0
votes
2
replies
229
views
featureCounts output summary assigned value higher than uniquely mapped reads from HISAT2
RNA-seq
featureCounts
HISAT
updated 1 day ago by
i.sudbery
19k • written 1 day ago by
Prawesh
• 0
3
votes
2
replies
1.2k
views
DESeq2 design and Batch effects
RNA-Seq
batch-effect
DESeq2
updated 23 days ago by
Ram
43k • written 4.4 years ago by
baldissera152
▴ 10
1
vote
2
replies
312
views
Tumour purity and ploidy estimation
Copy-number
Whole-exome-sequencing
24 days ago by
bp22
▴ 80
0
votes
2
replies
2.8k
views
RNA-seq unbalanced batch effect correction
limma
RNA-Seq
edgeR
batch-effect
updated 21 days ago by
Ram
43k • written 7.0 years ago by
endikavarela
• 0
0
votes
2
replies
218
views
What should I consider as FASTA for dataset?
PDB
FASTA
10 days ago by
Nafi
• 0
1
vote
2
replies
822
views
What type of normalization does removeBatchEffect function require as the input?
batch
limma
removeBatchEffect
rna-seq
batch-effect
updated 23 days ago by
Ram
43k • written 21 months ago by
ev97
▴ 20
0
votes
2
replies
579
views
How to get the reference panel for UKBB
UKBB
GWAS
clump
21 days ago by
航太郎
• 0
420 results • Page
3 of 9
Recent Votes
Comment: samtools tview symbols
Answer: Server or aws cloud- which one is better for gatk pipeline
Comment: Question about methylation location
Comment: Question about methylation location
Comment: Question about methylation location
How to use minimap2?
Comment: RNA seq analysis
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Recent Replies
Comment: In IGV is this a heterogeneous mutation or false call?
by
Tuck898
• 0
Ah I've just found 'show soft clipped bases' and this is what comes up... how come it is all greyed out? ![enter image description here][…
Comment: In IGV is this a heterogeneous mutation or false call?
by
Tuck898
• 0
I've just displayed clipped bases and this is what it shows. Does this look right? ![enter image description here][1] ![enter imag…
Comment: In IGV is this a heterogeneous mutation or false call?
by
Tuck898
• 0
Hi, I really appreciate you taking the time to reply. I'm still learning with IGV and sorry to sound very inexperienced but how would I che…
Answer: In IGV is this a heterogeneous mutation or false call?
by
Pierre Lindenbaum
161k
there is a clear shift in the depth just close to this mutation, you should set IGV to display the clipped bases + check if there is a DUP …
Comment: Too many unpaired forward reads found by Trimmomatic
by
SilhouetteQ
• 0
Using fastp, I found that the adapter sequence for the forward read is corresponding to Trans2_rc in the NexteraPE-PE.fa, while for the re…
Comment: cellranger error message
by
Max
• 0
I think the problem is your fastq_id. This should also read "RabhiN_PHLGEX". Hope this helps!
Comment: How to format "I" and "D" in vcf version 4.2 for liftover analysis in GATK
by
Giulio Genovese
▴ 390
@yokofakun is correct. Also, do notice that the GATK option `--RECOVER_SWAPPED_REF_ALT True` does not work with indels. In general, if your…
Comment: How to format "I" and "D" in vcf version 4.2 for liftover analysis in GATK
by
Pierre Lindenbaum
161k
> Don't forget to follow up on your threads. If an answer was helpful, you should upvote it; if the answer resolved your question, you shou…
Comment: How to format "I" and "D" in vcf version 4.2 for liftover analysis in GATK
by
Pierre Lindenbaum
161k
I think this is useless, in the gatk doc: > For each variant, the tool will look for the target coordinate, reverse-complement and left-al…
Comment: Too many unpaired forward reads found by Trimmomatic
by
GenoMax
142k
Ideally you will know which adapters to use but if you don't then programs like `fastp` can auto-detect them. You could also use `bbduk.sh`…
Comment: UMI-Tools knee-method has great influence on the results of white list
by
i.sudbery
19k
With the `--read2-only` option (which isn't available yet on the bioconda version), this will complain about a lack of `--bc-pattern`. How…
Comment: samtools tview symbols
by
Ruqaiya
• 0
What does the star mean then ?
Comment: RNA seq analysis
by
prifa
▴ 10
it's raw data **fastq.gz**, so for example I have 4 different samples from different tissue, sample A with 3 replicates, samples B,C and D …
Answer: Filtering Multi-sample VCF file for all except one Genotype
by
Pierre Lindenbaum
161k
> The goal is to remove all the variants which are unique to the KWSBambina sample. using jvarkit vcffilterjdk https://jvarkit.readthedo…
Comment: Too many unpaired forward reads found by Trimmomatic
by
SilhouetteQ
• 0
The first example used the adapter file NexteraPE-PE.fa, but it generated more than 50% unpaired data...... The content of NexteraPE-PE.fa…
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