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142 results • Page
1 of 3
Sort: replies
Rank
Views
Votes
Replies
3
votes
16
replies
9.9k
views
combining z-scores into a single z-score value
excel
R
statistics
updated 3 days ago by
Ram
39k • written 4.2 years ago by
Star
▴ 60
3
votes
12
replies
2.1k
views
What is NCBI Gene ID, where to find it and how to convert to entrez ID?
RNA-Seq
updated 23 hours ago by
Pegasus
▴ 90 • written 3.7 years ago by
mnazir
▴ 10
1
vote
10
replies
2.5k
views
How to specify/calculate subject coverage of the alignment (alignment of query[protein sequence] and subject[Nucleotide sequence]) in tBLASTn?
alignment
BLAST
tBLASTn
updated 6 days ago by
Ram
39k • written 4.2 years ago by
Kumar
▴ 100
0
votes
8
replies
286
views
The inchworm process failed. Trinity running error.
inchworm
transcriptome
trinity
updated 8 hours ago by
GenoMax
129k • written 1 day ago by
Marta
• 0
0
votes
7
replies
546
views
How to deal with duplicated gene IDs in TCGA RNA expression data?
TCGA
Expression
mRNA
updated 2 days ago by
Vincent Laufer
★ 2.9k • written 6 days ago by
Camilo Andres
▴ 30
1
vote
7
replies
5.6k
views
Human reference files in HG38 GATK resource bundle
VCF
updated 3 days ago by
dare_devil
★ 3.1k • written 5.3 years ago by
win
▴ 940
4
votes
7
replies
2.2k
views
low bootstrap value?
phylogeny
genome
alignment
updated 1 day ago by
Ram
39k • written 4.0 years ago by
Kumar
▴ 100
3
votes
7
replies
1.1k
views
Find 3'UTRs for species
Assembly
alignment
updated 5 minutes ago by
Ram
39k • written 3.8 years ago by
Palgrave
▴ 110
7
votes
7
replies
4.4k
views
RNA-Seq time series analysis using a DESeq2 spline approach yields far too many significant genes
splines
DESeq2
time-series
RNA-Seq
updated 3 days ago by
Ram
39k • written 4.4 years ago by
stu111538
▴ 80
2
votes
6
replies
1.0k
views
Time series RNA seq design query
RNA-seq
time-series
deseq2
updated 3 days ago by
Ram
39k • written 18 months ago by
kra277
• 0
0
votes
6
replies
333
views
Demultiplexing bam file
demultiplexing
bam_file
Iontorrent
4 days ago by
hasani.iut6
▴ 60
4
votes
6
replies
1.4k
views
Why weblogo of biopython doesn't work?
Biopython
Weblogo
updated 17 hours ago by
minakshiboruahassam
• 0 • written 9 months ago by
Plus
▴ 20
2
votes
5
replies
402
views
Cutadapt error: too many parameters.
cutadapt
parallel
bash
3 days ago by
DanielEB_fisk
• 0
1
vote
5
replies
2.3k
views
Calculating distance matrix of RNA-seq data
Dynamic-Time-Warping
R
time-series
updated 3 days ago by
Ram
39k • written 5.2 years ago by
fi1d18
★ 4.2k
1
vote
5
replies
3.6k
views
Time-series or pairwise comparison EdgeR - what's more suited?
DGE-analysis
Time-series
pairwise
updated 3 days ago by
Ram
39k • written 6.8 years ago by
Biogeek
▴ 470
0
votes
5
replies
700
views
vcftools --weir-fst-pop returns -nan
fst
vcftools
updated 3 days ago by
mingxi
• 0 • written 5 months ago by
elizabeth
• 0
5
votes
4
replies
1.5k
views
Detection of DE genes among different tissues of an organism during time - RNA seq
detection
DE-genes
multi-treatments
time-series
updated 3 days ago by
Ram
39k • written 6.9 years ago by
statfa
▴ 720
3
votes
4
replies
216
views
Does adding reads cause batch effects?
kallisto
RNAseq
updated 22 hours ago by
ATpoint
72k • written 1 day ago by
bioinfo
▴ 80
0
votes
4
replies
215
views
Identification of genes involved in my pathway
KEGG
keggGet
21 hours ago by
smanzano250800
• 0
1
vote
4
replies
1.5k
views
Time series event recurrence comparison
recurrence
time-series
updated 3 days ago by
Ram
39k • written 6.7 years ago by
Nicolas Rosewick
10k
1
vote
4
replies
350
views
Pre-processing for Agilent microarray data?
affymetrix
microarray
gene
agilent
rna
updated 5 days ago by
solarchan7
• 0 • written 10 days ago by
survive
• 0
0
votes
4
replies
788
views
Detecting Biomarkers from Time Series Gene Epression data
Time-Series
Gene-Expression
Biomarkers
updated 3 days ago by
Ram
39k • written 3.1 years ago by
donnieDarko
• 0
0
votes
4
replies
145
views
how to Construct a Newick tree file from five large fasta files
tree
Newick
alignment
updated 46 minutes ago by
Ram
39k • written 8 hours ago by
gunala.nikhil
• 0
4
votes
4
replies
342
views
Segmentation fault Biopython pairwise alignment
biopython
alignment
updated 3 days ago by
Joe
21k • written 7 days ago by
antoine.fauchois92
▴ 20
0
votes
4
replies
331
views
desgin a primer for CDS
gene
pcr
6 days ago by
yuxiang
• 0
2
votes
4
replies
222
views
Filter VCF file for variant alleles
VCF
variants
bcftools
vcftools
updated 1 day ago by
Ram
39k • written 2 days ago by
miguellarrazlopezdenovales
• 0
0
votes
4
replies
276
views
I need help with a methyl array data analysis
methyl_array
DMPs
DMRs
beta_value
r
5 days ago by
Ahmad
▴ 10
1
vote
3
replies
174
views
My kernel is killing the pairtools dedup script, how to prevent that?
ubuntu
hic
pairtools
aws
updated 1 day ago by
GenoMax
129k • written 1 day ago by
NikhilP
▴ 20
0
votes
3
replies
218
views
Query qbout single cell sequencing
fastq
ScRNA
updated 3 days ago by
Ram
39k • written 4 days ago by
abbas.waseem.gcu
▴ 20
2
votes
3
replies
1.2k
views
mutational signatures in different tumor samples
somatic mutation
mutational signature
updated 1 day ago by
Vincent Laufer
★ 2.9k • written 4.4 years ago by
lzy
▴ 20
0
votes
3
replies
185
views
Dada2 in Qiime2: losing reads during merging
Qiime2
Chimer
Dada2
updated 2 days ago by
andres.firrincieli
3.3k • written 3 days ago by
kamanovae
▴ 80
0
votes
3
replies
173
views
minimap's SAM file MAPQ value for the unique alignments
minimap
MAPQ
RNAseq
1 day ago by
Mohd
▴ 20
1
vote
3
replies
161
views
How to get a comperative result of 2 bed files?
bam
cnv
bed
updated 1 day ago by
Pierre Lindenbaum
154k • written 2 days ago by
herh
• 0
0
votes
3
replies
96
views
hardfilter error
bam
recall
7 hours ago by
bestone
▴ 10
0
votes
3
replies
453
views
how to calcul risk score with a prognostic genes
riskscore
multivariate
analysis
prognostic
model
updated 6 days ago by
Maryam
• 0 • written 8 months ago by
Nobody
▴ 30
0
votes
3
replies
719
views
How can I use KING on windows ?
plink
king
updated 2 days ago by
Ram
39k • written 4.0 years ago by
gwas_maniac
▴ 20
2
votes
3
replies
690
views
Including bioinformatics into an agriculture/horticulture dissertation project
agrobioinformatics
plant-gene-analysis
updated 2 days ago by
Ram
39k • written 4.1 years ago by
cipri91rusu
• 0
1
vote
3
replies
205
views
To call variants can I use my aligned WGS data as a reference genome
VCF
samtools
reference
genome
updated 1 day ago by
GenoMax
129k • written 1 day ago by
mls
• 0
0
votes
3
replies
136
views
convert data frame with character column to data frame with integer column
r
updated 5 hours ago by
Basti
★ 1.5k • written 12 hours ago by
atemedorri137798
• 0
0
votes
3
replies
159
views
DEGseq for multiple samples
DEGseq
DEG
updated 1 day ago by
Ram
39k • written 1 day ago by
ALOUSH ALI
• 0
1
vote
3
replies
698
views
Regular Expression for conversion
Linux
grep
updated 3 days ago by
Joe
21k • written 19 months ago by
shabbas12
▴ 10
1
vote
2
replies
133
views
The famous WGS dataset, Ashkenazi Trio?
wgs
dataset
updated 3 hours ago by
thadjudkins2
• 0 • written 17 hours ago by
herh
• 0
0
votes
2
replies
175
views
how to look for interactions between different chromosomes
SNP
interactions
Gene
HiC
22 hours ago by
rheab1230
▴ 140
0
votes
2
replies
169
views
fgsea/clusterProfiler Packages for nCounter data enrichment analysis
nanostring
gsea
r
4 days ago by
pg45863
• 0
0
votes
2
replies
214
views
BCR/TCR analysis using target capture sequencing data
capture
ngs
TCR
BCR
2 days ago by
J.F.Jiang
▴ 900
1
vote
2
replies
254
views
DEgs RNAseq
RNAseq
5 days ago by
Juan
• 0
0
votes
2
replies
195
views
Upstream pseudogene causing MAPQ 0 and exclusion during variant calling
Mapping
Variant-calling
masking
updated 4 days ago by
Ram
39k • written 4 days ago by
Joel Wallenius
▴ 130
1
vote
2
replies
195
views
Converting RefSeq protein accession IDs into entreZ IDs
RNA-SEQ
2 days ago by
Pegasus
▴ 90
0
votes
2
replies
146
views
readGenericHeader() error message Limma
rna
limma
microarray
genomics
normalization
1 day ago by
survive
• 0
0
votes
2
replies
519
views
1-way-2-fold cross family analysis
cross-family-analysis
updated 2 days ago by
Ram
39k • written 3.8 years ago by
sinha.shriprakash
▴ 20
142 results • Page
1 of 3
Recent Votes
Answer: What does canonical transcript mean in the context of VEP
Automated dbSNP lookup by rsID position, plus genome build liftover
Relatedness vs relatedness2 from vcftools give different results
A: Relatedness vs relatedness2 from vcftools give different results
Comment: LDheatmap will not accept LD matrix from Plink
LDheatmap will not accept LD matrix from Plink
A: mitochondrial/ribosomal protein genes in scRNA-seq analysis
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Comment: What does canonical transcript mean in the context of VEP
by
Ram
39k
> Does that mean the fully functional gene most folks think of when thinking of their favorite gene? That ... doesn't make much sense. Did…
Answer: What does canonical transcript mean in the context of VEP
by
Pierre Lindenbaum
154k
https://www.ensembl.org/info/genome/genebuild/canonical.html > The Ensembl Canonical transcript is a single, representative transcript ide…
Answer: Why is coordinate sort required before findng read depths?
by
Ram
39k
In an unsorted BAM file, reads can be in any random order. In a co-ordinate sorted BAM file, reads are in the order in which they map to th…
Comment: What is "pident" (percentage of identical matches) in the "Diamond" protein alig
by
Alexander
▴ 70
how does it correspond to 27.2 ? or these are the other proteins ?
Comment: Merge different vcf files
by
Ram
39k
Normalize them first using `vt normalize` or `bcftools norm` - they need to be in left-aligned parsimonious representation before you can d…
Answer: integrate single cell RNA sequencing data
by
John Ma
▴ 300
You need to perform batch effect removal for these. Seurat has its integration protocol, and if you use scverse on Python, the usual choice…
Comment: What is "pident" (percentage of identical matches) in the "Diamond" protein alig
by
GenoMax
129k
I added the link for NCBI "book" since DIAMOND seems to follow the format/reporting structure for blast+ results. While the numbers shown i…
Comment: bcftools "--filter-logic" flag, what + means?
by
Ram
39k
`PASS` + `filter_name` is `filter_name`, not `PASS,filter_name`. PASS means the locus hit no filter. You'll never see a `PASS,<something>`.…
Comment: What is "pident" (percentage of identical matches) in the "Diamond" protein alig
by
Alexander
▴ 70
Thank you for the reply ! I got seems to be even more puzzled here - we see "identities" 95% while in the example "pident" is 27.2 - so …
Comment: bcftools "--filter-logic" flag, what + means?
by
Eugene A
▴ 170
Thanks a lot for the explanation!
Comment: How GATK pipeline called a homozygeous alternate allele (1/1) although one copy
by
Ram
39k
> Do you mean that because it is 1/1, so both copies is different from the reference and that is why the 0 in the AD is because no reads is…
Comment: What is "pident" (percentage of identical matches) in the "Diamond" protein alig
by
Alexander
▴ 70
Thank you ! @buchfink would you be so kind to comment ?
Comment: The famous WGS dataset, Ashkenazi Trio?
by
thadjudkins2
• 0
As the previous poster said we’re not sure what you’re looking for, but the basic data are available at the NCBI ftp site (linked from the …
Comment: Retrieving allele-specific information for a variant using VEP annotation
by
bt_cepo
▴ 20
Thank you both for your answers @masklin @ram ! For anyone facing the same problem, I followed Ram's suggestions and it worked beautifully…
Comment: how to Construct a Newick tree file from five large fasta files
by
gunala.nikhil
• 0
I need a phylogenetic tree for those 5 genomes
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