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32 results • Page
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7
votes
17
replies
1.1k
views
Building reference dbSNP file using WGS samples
NGS
WGS
Variant-calling
non-model
Bootstrapping
11 hours ago by
analyst
▴ 10
4
votes
15
replies
6.4k
views
8 follow
bbmap split paired-end reads back into separated fastq files?
genome
next-gen-sequencing
bbmap
alignment
updated 20 hours ago by
GenoMax
136k • written 5.2 years ago by
c.e.chong
▴ 60
4
votes
11
replies
6.0k
views
6 follow
Installing and importing viennaRNA to python in windows
rna
python
viennarna
updated 20 hours ago by
Yun
• 0 • written 4.3 years ago by
ofek.schnitzer
▴ 30
1
vote
10
replies
1.8k
views
Scanpy Pearson residual PCA error
python
scRNA
scanpy
PCA
updated 8 hours ago by
Maëlick
• 0 • written 15 months ago by
Emily
▴ 70
0
votes
6
replies
196
views
Resolving over clustered NGS with Q-scores
NGS
phred
Q-score
overclustering
1 hour ago by
sam.himes92
• 0
1
vote
5
replies
817
views
Strandedness of RNA-seq results
dual-RNA-seq
featurecounts
strandedness
HISAT2
updated 17 hours ago by
charles.feigin
• 0 • written 18 months ago by
jamesymtang
▴ 10
4
votes
5
replies
295
views
Calculate GC content for entire chromosome
bam
GC
assembly
bwa-mem
updated 7 hours ago by
colindaven
5.8k • written 1 day ago by
skilleta0527
• 0
2
votes
4
replies
283
views
An issue with gtf file (ballgownrsem)
Ballgown
RNA-seq
GTF
RSEM
8 hours ago by
cucindarko51
• 0
2
votes
4
replies
594
views
Genome coverage of MAGs while submitting to NCBI
genome
MAGs
coverage
metagenomics
updated 21 hours ago by
wn835166087
• 0 • written 3 months ago by
Konstantin
• 0
0
votes
4
replies
657
views
How to resolve the error of protein lacking a stop codon when using GenomeThreader for homology prediction?
genome
threader
21 hours ago by
peanut
• 0
1
vote
4
replies
198
views
Feasibility of Enrichment Analysis from RTqPCR results
GO
RT-qPCR
Enrichment-Analysis
updated 16 hours ago by
GenoMax
136k • written 1 day ago by
Javier
• 0
0
votes
4
replies
220
views
Need help to find FASTA sequence from dbSNP
dbSNP
SNP
FASTA
updated 9 hours ago by
GenoMax
136k • written 15 hours ago by
syedahumairagillani
• 0
5
votes
4
replies
6.0k
views
How is "integer score for display" calculated in MACS2
ChIP-Seq
MACS2
narrowPeak
updated 6 hours ago by
SplitInf
▴ 10 • written 7.2 years ago by
Vanilla
▴ 110
0
votes
4
replies
57
views
Where can I get a list of SNPs mapping overlapping genes in humans?
SNPs
updated 1 hour ago by
Alex Reynolds
35k • written 2 hours ago by
Mr Locuace
▴ 150
0
votes
3
replies
94
views
Annotation Visualization IGV
igv
alignment
gff
annotation
visualization
updated 3 hours ago by
Pierre Lindenbaum
158k • written 3 hours ago by
awhale01
• 0
0
votes
2
replies
180
views
Issues while running blastx
blastx
RNA-seq
updated 16 hours ago by
GenoMax
136k • written 1 day ago by
Foad
▴ 10
3
votes
2
replies
148
views
Execute R command on specific termimal
R
updated 7 hours ago by
Ram
41k • written 12 hours ago by
QX
• 0
0
votes
2
replies
121
views
Very low successfully assigned alignments with feature counts
featureCounts
RNA-seq
updated 6 hours ago by
Istvan Albert
99k • written 8 hours ago by
Manuel
• 0
1
vote
2
replies
298
views
Best method for batch correction of three datasets
RNA-seq
updated 15 hours ago by
ATpoint
78k • written 1 day ago by
CTLong
▴ 20
4
votes
2
replies
172
views
Ambient RNA removal method that generates whole (integer) counts
pseudobulk
soupX
DESeq2
single-cell
3 hours ago by
EK
• 0
0
votes
1
reply
129
views
Cell ranger multi for demultiplexing FB files and GEX files
cellranger
updated 7 hours ago by
Ram
41k • written 1 day ago by
Shloka
• 0
0
votes
1
reply
47
views
How to add exon annotations to genome annotation
proteome
genome
BED
annotation
updated 2 hours ago by
alex.zaccaron
▴ 380 • written 2 hours ago by
Simone
▴ 10
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 17 hours ago by
charles.feigin
• 0 • written 6 weeks ago by
xinrantian
▴ 20
0
votes
1
reply
127
views
Software for Spatial Transcriptomic data [NanoString; Visium]?
NanoString
Visium
Spatial-Transcriptomics
10X
21 hours ago by
LauferVA
3.8k
0
votes
1
reply
126
views
Aligning sequences with multiple genetic codes!
genetic_codes
codon
MEGA11
alignment
updated 7 hours ago by
5heikki
11k • written 23 hours ago by
George X.
• 0
0
votes
1
reply
91
views
Curated model organism gene functional annotations
Interpro
C.elegans
GO-terms
updated 7 hours ago by
Ram
41k • written 8 hours ago by
ian.will
▴ 10
1
vote
1
reply
155
views
How to use Nextflow to call scripts from different environments?
anaconda
conda
nextflow
updated 7 hours ago by
Ram
41k • written 23 hours ago by
O.rka
▴ 710
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
3 hours ago by
supernovamik
• 0
0
votes
0
replies
29
views
News:
University of Connecticut Single Cell RNA-seq Workshop December 12-15, 2023
expression
singlecell
rnaseq
2 hours ago by
mia.nahom
▴ 10
0
votes
0
replies
68
views
megablast taxonomy assign in blobtools
blobtools
20 hours ago by
bs
• 0
0
votes
0
replies
61
views
ASEReadCounter output wrong number of coverage
ASEReadCounter
17 hours ago by
junhuili
• 0
0
votes
0
replies
54
views
Tutorial:
CITEseq tutorial
CITEseq
Alevin
Seurat
8 hours ago by
Ming Tommy Tang
★ 3.6k
32 results • Page
1 of 1
Recent Votes
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?
C: visualizing mutational data using Maftools for reference genome hg19
Answer: Ambient RNA removal method that generates whole (integer) counts
Answer: Ambient RNA removal method that generates whole (integer) counts
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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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