Latest
Open
Jobs
Tutorials
Tags
About
FAQ
Community
Planet
New Post
Log In
New Post
Latest
Open
News
Jobs
Tutorials
Forum
Tags
Planet
Users
Log In
Sign Up
About
Limit : today
all time
today
this week
this month
this year
32 results • Page
1 of 1
Sort: replies
Rank
Views
Votes
Replies
7
votes
17
replies
1.1k
views
Building reference dbSNP file using WGS samples
NGS
WGS
Variant-calling
non-model
Bootstrapping
13 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 21 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 22 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 10 hours ago by
Maëlick
• 0 • written 15 months ago by
Emily
▴ 70
0
votes
6
replies
227
views
Resolving over clustered NGS with Q-scores
NGS
phred
Q-score
overclustering
2 hours ago by
sam.himes92
• 0
1
vote
5
replies
820
views
Strandedness of RNA-seq results
dual-RNA-seq
featurecounts
strandedness
HISAT2
updated 18 hours ago by
charles.feigin
• 0 • written 18 months ago by
jamesymtang
▴ 10
4
votes
5
replies
303
views
Calculate GC content for entire chromosome
bam
GC
assembly
bwa-mem
updated 9 hours ago by
colindaven
5.8k • written 1 day ago by
skilleta0527
• 0
2
votes
4
replies
286
views
An issue with gtf file (ballgownrsem)
Ballgown
RNA-seq
GTF
RSEM
9 hours ago by
cucindarko51
• 0
2
votes
4
replies
594
views
Genome coverage of MAGs while submitting to NCBI
genome
MAGs
coverage
metagenomics
updated 22 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
22 hours ago by
peanut
• 0
1
vote
4
replies
200
views
Feasibility of Enrichment Analysis from RTqPCR results
GO
RT-qPCR
Enrichment-Analysis
updated 18 hours ago by
GenoMax
136k • written 1 day ago by
Javier
• 0
0
votes
4
replies
224
views
Need help to find FASTA sequence from dbSNP
dbSNP
SNP
FASTA
updated 10 hours ago by
GenoMax
136k • written 17 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 7 hours ago by
SplitInf
▴ 10 • written 7.2 years ago by
Vanilla
▴ 110
1
vote
4
replies
103
views
Where can I get a list of SNPs mapping overlapping genes in humans?
SNPs
updated 2 hours ago by
Alex Reynolds
35k • written 3 hours ago by
Mr Locuace
▴ 150
2
votes
3
replies
113
views
Annotation Visualization IGV
igv
alignment
gff
annotation
visualization
updated 4 hours ago by
Pierre Lindenbaum
158k • written 4 hours ago by
awhale01
• 0
0
votes
2
replies
182
views
Issues while running blastx
blastx
RNA-seq
updated 18 hours ago by
GenoMax
136k • written 1 day ago by
Foad
▴ 10
4
votes
2
replies
154
views
Execute R command on specific termimal
R
updated 8 hours ago by
Ram
41k • written 14 hours ago by
QX
• 0
0
votes
2
replies
126
views
Very low successfully assigned alignments with feature counts
featureCounts
RNA-seq
updated 7 hours ago by
Istvan Albert
99k • written 10 hours ago by
Manuel
• 0
1
vote
2
replies
301
views
Best method for batch correction of three datasets
RNA-seq
updated 16 hours ago by
ATpoint
78k • written 1 day ago by
CTLong
▴ 20
4
votes
2
replies
184
views
Ambient RNA removal method that generates whole (integer) counts
pseudobulk
soupX
DESeq2
single-cell
5 hours ago by
EK
• 0
0
votes
1
reply
131
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
1
reply
66
views
How to add exon annotations to genome annotation
proteome
genome
BED
annotation
updated 3 hours ago by
alex.zaccaron
▴ 380 • written 3 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 18 hours ago by
charles.feigin
• 0 • written 6 weeks ago by
xinrantian
▴ 20
0
votes
1
reply
132
views
Software for Spatial Transcriptomic data [NanoString; Visium]?
NanoString
Visium
Spatial-Transcriptomics
10X
22 hours ago by
LauferVA
3.8k
0
votes
1
reply
130
views
Aligning sequences with multiple genetic codes!
genetic_codes
codon
MEGA11
alignment
updated 9 hours ago by
5heikki
11k • written 1 day ago by
George X.
• 0
0
votes
1
reply
98
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
1
vote
1
reply
159
views
How to use Nextflow to call scripts from different environments?
anaconda
conda
nextflow
updated 8 hours ago by
Ram
41k • written 1 day 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
4 hours ago by
supernovamik
• 0
0
votes
0
replies
44
views
News:
University of Connecticut Single Cell RNA-seq Workshop December 12-15, 2023
expression
singlecell
rnaseq
4 hours ago by
mia.nahom
▴ 10
0
votes
0
replies
70
views
megablast taxonomy assign in blobtools
blobtools
21 hours ago by
bs
• 0
0
votes
0
replies
63
views
ASEReadCounter output wrong number of coverage
ASEReadCounter
19 hours ago by
junhuili
• 0
0
votes
0
replies
56
views
Tutorial:
CITEseq tutorial
CITEseq
Alevin
Seurat
10 hours ago by
Ming Tommy Tang
★ 3.6k
32 results • Page
1 of 1
Recent Votes
Comment: Annotation Visualization IGV
Comment: Annotation Visualization IGV
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?
Recent Locations •
All
China,
1 minute ago
Chile,
1 minute ago
United States,
5 minutes ago
United States,
7 minutes ago
Republic of Ireland,
8 minutes ago
Seattle, WA USA,
8 minutes ago
Memphis, TN,
8 minutes ago
Recent Awards •
All
Popular Question
to
samreen.jasvi
• 0
Teacher
to
h.mon
35k
Scholar
to
jared.andrews07
★ 16k
Popular Question
to
Mr Locuace
▴ 150
Popular Question
to
benjamin.pyenson
• 0
Popular Question
to
Malachi Griffith
19k
Popular Question
to
awhale01
• 0
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.
Traffic: 1365 users visited in the last hour
Content
Search
Users
Tags
Badges
Help
About
FAQ
Access
RSS
API
Stats
Use of this site constitutes acceptance of our
User Agreement and Privacy Policy
.
Powered by the
version 2.3.6