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88 results • Page
2 of 2
Sort: replies
Rank
Views
Votes
Replies
0
votes
1
reply
154
views
Contrasts in R
contrasts
r
updated 1 day ago by
jv
★ 1.3k • written 1 day ago by
SGMS
▴ 130
0
votes
1
reply
689
views
Alternative tool for split'N'trim
SNP
Galaxy
Single-cell
RNA-seq
updated 1 day ago by
Ram
41k • written 3.6 years ago by
aiswaryabioinfo
▴ 30
1
vote
1
reply
126
views
ANNOVAR Download Failing
ANNOVAR
updated 1 day ago by
Ram
41k • written 1 day ago by
tony
• 0
0
votes
1
reply
134
views
Sorted bam files are empty after sorting them from bam
bam
dna
updated 1 day ago by
Ram
41k • written 1 day ago by
mgranada3
▴ 30
0
votes
1
reply
131
views
Software for Spatial Transcriptomic data [NanoString; Visium]?
NanoString
Visium
Spatial-Transcriptomics
10X
22 hours ago by
LauferVA
3.8k
1
vote
1
reply
1.0k
views
How to interpret the discrepancy of assignment rate in featurecounts using forward and reverse strand protocols
RNAseq
updated 18 hours ago by
charles.feigin
• 0 • written 6 weeks ago by
xinrantian
▴ 20
0
votes
1
reply
128
views
Aligning sequences with multiple genetic codes!
genetic_codes
codon
MEGA11
alignment
updated 8 hours ago by
5heikki
11k • written 1 day ago by
George X.
• 0
0
votes
1
reply
97
views
Curated model organism gene functional annotations
Interpro
C.elegans
GO-terms
updated 8 hours ago by
Ram
41k • written 9 hours ago by
ian.will
▴ 10
0
votes
1
reply
130
views
Cell ranger multi for demultiplexing FB files and GEX files
cellranger
updated 8 hours ago by
Ram
41k • written 1 day ago by
Shloka
• 0
0
votes
0
replies
98
views
Enzyme commission number in ncbi Gene database
enzyme-commission-number
updated 1 day ago by
Ram
41k • written 1 day ago by
Maatary
• 0
0
votes
0
replies
688
views
Generating variant read count matrix, total read count matrix and binary/ternary mutaion matrix for SNV from scDNAseq FASTQ files
SNV
mutationMatrix
tumorPhylogeny
scDNAseq
mutaion
4 hours ago by
supernovamik
• 0
0
votes
0
replies
196
views
Trouble Adding Log Fold Changes to KEGG Pathway Visualization
KEGG
RStudio
updated 2 days ago by
Ram
41k • written 26 days ago by
ramirj49
• 0
0
votes
0
replies
77
views
spatial metabolomics, python
spatial-metabolomics
updated 1 day ago by
Ram
41k • written 1 day ago by
joha
▴ 10
0
votes
0
replies
202
views
How to find promoters (such as GC box and TATA box) in set of genes using bioinformatics analysis ?
promoter
motif
updated 2 days ago by
Ram
41k • written 5 days ago by
shome
▴ 10
0
votes
0
replies
86
views
extracting Uniprot IDs for Kegg pathways
mapping
uniprot
R
kegg
clusterprofiler
2 days ago by
Assa Yeroslaviz
★ 1.8k
0
votes
0
replies
115
views
Should I perform eQTL colocalization for just one of eGenes at a time?
colocalization
coloc
eCaviar
eQTL
3 days ago by
maximal_life
▴ 20
0
votes
0
replies
112
views
BioSQL Unable to remove database using server.remove_database
BioSQL
biopython
Mysql
Python
4 days ago by
Navindu
• 0
0
votes
0
replies
130
views
how to download the VCF/MAF files from cBioportal genie site
cBioportal
mutation
VCF
TMB
6 days ago by
luckyday1661
• 0
0
votes
0
replies
125
views
bootstraped treemix show no migration event
Treemix
Bootstrap
4 days ago by
reza
▴ 300
0
votes
0
replies
131
views
How to do KEGG pathway analysis when I have a gene with multiple entrez IDs?
biomart
kegg
deseq2
6 days ago by
bioinfo
▴ 140
0
votes
0
replies
103
views
how to calculate intramodular connectivity
WGCNA
intramodularConnectivity
6 days ago by
hellokwmin
• 0
0
votes
0
replies
146
views
is there a way to set colors pallets for glMDSPlot(x)?
Glimma
glMDSPlot
5 days ago by
James
• 0
0
votes
0
replies
94
views
Differing output: vcftools' --weir-fst-pop and R hierfstats package's varcomp.glob()
vcftools
hierfstats
fst
2 days ago by
S
• 0
0
votes
0
replies
109
views
Expression differs when running plotTranscripts vs boxplot of FPKM or coverage values (R)?
R
updated 2 days ago by
Ram
41k • written 2 days ago by
boone5jones
• 0
0
votes
0
replies
131
views
Compute matrix skipping many regions stating not found in compute matrix output
computematrix
Deeptools
5 days ago by
Mehwish
▴ 10
0
votes
0
replies
158
views
Significance of several BUSCO target IDs for the same gene
target_id
sequence-ontology
BUSCO
duplication
5 days ago by
CoLa
• 0
0
votes
0
replies
93
views
GAPIT p-value significance threshold
GAPIT
p-value
GWAS
1 day ago by
Clayton
• 0
0
votes
0
replies
146
views
Osmotic permeability of water transport in aquaporins
permeability
Osmotic
transport
Water
5 days ago by
Peerzada
• 0
0
votes
0
replies
92
views
Comparing 16S rRNA (culture) sequences with metagenome
metagenome
shotgun
rRNA_culture
16S
updated 2 days ago by
Ram
41k • written 2 days ago by
aswin
• 0
0
votes
0
replies
80
views
How do I pick the best conditions for scATAC-Seq after a series of bulk test runs?
ATAC-seq
2 days ago by
cyril-cros
▴ 940
0
votes
0
replies
86
views
Need to PrepSCTfindMarker again after subset if the original object has already been normalized?
FindMarker
Seurat
1 day ago by
Adrian
• 0
0
votes
0
replies
89
views
RNA secondary structure for GRCH38 transcriptome
dot-bracket-notation
human
RNA-secondary-structure
GRCH38
1 day ago by
Saad Khan
▴ 420
0
votes
0
replies
99
views
Classification ML model using different type of data
machine-learning
transcriptomics
R
python
biomarkers
1 day ago by
sil_bioinfo
▴ 40
0
votes
0
replies
97
views
ADMIXTURE Freezes Right Before Completion
ADMIXTURE
admixture
6 days ago by
maxlaubstein
• 0
0
votes
0
replies
146
views
Extract upstream and downstream 50bp nontemplated sequences from a position
search
sequences
nontemplated
motif
6 days ago by
Ty
• 0
0
votes
0
replies
92
views
WGCNA for different tissues
WGCNA
Worms
RNA-Seq
1 day ago by
kdca
• 0
0
votes
0
replies
69
views
megablast taxonomy assign in blobtools
blobtools
21 hours ago by
bs
• 0
0
votes
0
replies
62
views
ASEReadCounter output wrong number of coverage
ASEReadCounter
18 hours ago by
junhuili
• 0
88 results • Page
2 of 2
Recent Votes
Answer: Execute R command on specific termimal
Answer: Where can I get a list of SNPs mapping overlapping genes in humans?
Comment: How do I know how much memory to use when piping to with BBMap suite (OutOfMemor
A: difference between GSEA and Gene Ontology
Answer: Does the Minion demultiplex when basecalling?
the difference between the positions called by somatic caller (MuTect2) and the position called by germline caller (UnifiedGenotyper)?
A: Extract somatic mutations and germline mutations from variant calling files?
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Recent Awards •
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Popular Question
to
samreen.jasvi
• 0
Teacher
to
h.mon
35k
Scholar
to
jared.andrews07
★ 16k
Popular Question
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Mr Locuace
▴ 150
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benjamin.pyenson
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awhale01
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Recent Replies
Comment: Resolving over clustered NGS with Q-scores
by
sam.himes92
• 0
The system that we used was [Aviti][1]. Our sequencing core was the one who quantified the loading/library concentration. Sorry I don't hav…
Comment: Where can I get a list of SNPs mapping overlapping genes in humans?
by
Alex Reynolds
35k
I modified the answer with an approach for that use case.
Comment: Where can I get a list of SNPs mapping overlapping genes in humans?
by
Ram
41k
OP is looking for overlapping genes - genes with presumably different gene IDs that share some loci. I think the `genes.bed` creation logic…
Comment: Where can I get a list of SNPs mapping overlapping genes in humans?
by
Alex Reynolds
35k
Note: The file `snps.bed` will be very large. You'll need sufficient disk space for this step.
Answer: Where can I get a list of SNPs mapping overlapping genes in humans?
by
Alex Reynolds
35k
Given files `genes.bed` and `snps.bed`, you could do something like: ``` $ bedmap --echo --echo-map-id --delim '\t' genes.bed snps.bed > a…
Answer: How to add exon annotations to genome annotation
by
alex.zaccaron
▴ 380
You can use [AGAT][1] to process your annotation file to add the missing exons. I believe `agat_convert_sp_gxf2gxf.pl -g no_exons.gff -o wi…
Comment: Annotation Visualization IGV
by
Pierre Lindenbaum
158k
and you got answer that should be validate (green tick), or people asked you questions but got no answers.
Comment: Annotation Visualization IGV
by
awhale01
• 0
Correct I have asked those questions before.
Comment: Annotation Visualization IGV
by
Pierre Lindenbaum
158k
you asked questions before: review, comment and/or validate them please: https://www.biostars.org/p/9530777/ ; https://www.biostars.org/p/9…
Comment: Ambient RNA removal method that generates whole (integer) counts
by
EK
• 0
Thanks, Jared. Sounds like rounding counts is the simplest approach for now. :)
Comment: Resolving over clustered NGS with Q-scores
by
Trivas
★ 1.5k
Could you tell us which sequencer you used, how you quantified your library size and concentration, and what your loading concentration was…
Comment: Resolving over clustered NGS with Q-scores
by
sam.himes92
• 0
I should have mentioned, we ran both Read 1 and 2 well past the points of interest. For each read we ran 75 cycles.
Answer: Resolving over clustered NGS with Q-scores
by
Trivas
★ 1.5k
It might be because Illumina recommends 26 cycles for Read 1: https://knowledge.illumina.com/instrumentation/general/instrumentation-genera…
Comment: Resolving over clustered NGS with Q-scores
by
sam.himes92
• 0
Yes at 5%.
Comment: Resolving over clustered NGS with Q-scores
by
ATpoint
78k
Has phiX been spiked in to increase nucleotide diversity.
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