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 : this month
all time
today
this week
this month
this year
682 results • Page
2 of 14
Sort: Votes
Rank
Views
Votes
Replies
4
votes
0
replies
160
views
Herald:
The Biostar Herald for Monday, April 29, 2024
herald
19 days ago by
Biostar
2.8k
4
votes
9
replies
2.7k
views
Tool:
CANEapp, a user-friendly application for automated next generation transcriptomic data analysis
RNA-Seq
written 8.3 years ago by
dvelmeshev
• 0
4
votes
1
reply
205
views
Extracting only 4-fold degenerate sites from gene sequences/alignments?
alignments
4 days ago by
J.
▴ 40
4
votes
12
replies
4.9k
views
10 follow
How to analyze Infinium Mouse Methylation BeadChip array data?
Methylation
Experience
Illumina
Mouse
updated 9 days ago by
Tawny
▴ 180 • written 3.0 years ago by
julia_geh
▴ 20
4
votes
9
replies
2.1k
views
Legend and hap files for imputation with 38 build
reference
38build
impute
imputation
19 days ago by
anna
▴ 20
4
votes
1
reply
264
views
LD-prune variants while maintaining a list of SNPs
snp
vcf
plink
filtering
independent
updated 12 days ago by
zx8754
11k • written 14 days ago by
Jautis
▴ 560
4
votes
6
replies
1.2k
views
Soft-clipping read ends based on read group
ancient
molecule
at
bam
DNA
RG
ends
clipping
damage
updated 10 days ago by
chenl
▴ 10 • written 2.5 years ago by
Martyna
• 0
4
votes
6
replies
811
views
7 follow
Heatmap and rna-seq
RNA-Seq
Heatmap
updated 21 days ago by
dsull
★ 6.0k • written 25 days ago by
qudrat.nii
▴ 10
4
votes
6
replies
3.9k
views
Taking the difference of two VCFs (or removing singletons)
genome
sequencing
singleton
SNP
filter
updated 18 days ago by
Andres
▴ 20 • written 9.7 years ago by
hermathena
▴ 40
4
votes
7
replies
639
views
Very low RNA splicing rate for pulmonary AT2 cells
RNA-velocity
scVelo
scRNA-seq
splicing
19 days ago by
e.r.zakiev
▴ 210
4
votes
7
replies
480
views
In one PCA plot, can I calculate the percentage of different factors that contribute to the PCA?
PCA
R
VARIANCE
updated 1 day ago by
marco.barr
▴ 130 • written 3 days ago by
diqixiaoyaoer
▴ 20
4
votes
3
replies
2.9k
views
How to solve the error 'ERROR::MATE_NOT_FOUND:Found xxx unpaired mates' when run SamToFastq
samtofasq
picard
validatesamfile
updated 9 days ago by
Pierre Lindenbaum
161k • written 9 days ago by
Lila M
★ 1.2k
4
votes
5
replies
456
views
Figures are disappeared from html report of SnpEff
HTML
SnpEff
19 days ago by
analyst
▴ 50
4
votes
15
replies
1.7k
views
how to test for differential expression in samples where a global increase in gene expression is expected
edgeR
DESeq
Differential-Expression
RNA-Seq
updated 15 days ago by
Gordon Smyth
★ 7.2k • written 5 months ago by
raplayer
▴ 10
4
votes
4
replies
3.0k
views
CNVkit for somatic copy number detection
cnv
cnvkit
exome
WES
updated 4 days ago by
Anitha
• 0 • written 5.1 years ago by
stephaniem
• 0
4
votes
8
replies
773
views
Create a new bed file with all pairwise combinations between two other bed files, based on bp distance
SNPs
BED
eqtl
bedtools
updated 22 days ago by
Alex Reynolds
35k • written 22 days ago by
J
▴ 10
4
votes
1
reply
359
views
How to use limma to find differentially expressed genes in response to a continuous variable
limma
voom
R
19 days ago by
pairedttest
▴ 10
4
votes
3
replies
444
views
Source other conda environments in a nextflow pipeline when nextflow itself is in a conda environment?
hpc
conda
nextflow
updated 21 days ago by
Arup Ghosh
3.2k • written 22 days ago by
chaco001
▴ 40
4
votes
6
replies
3.8k
views
How to interpret DEXseq results in therms of significance
DEXseq
RNA-Seq
exon
updated 12 days ago by
Sara
▴ 30 • written 6.7 years ago by
Lila M
★ 1.2k
4
votes
7
replies
428
views
How does gene length effect the number of reads mapped
RNA-seq
CPM
sequencing
5 days ago by
Chen
• 0
4
votes
9
replies
2.2k
views
6 follow
Same sequencing sample in multiple lanes. How to analyse it?
sequencing
bowtie2
alignment
samtools
ngs
updated 15 days ago by
ST
• 0 • written 2.2 years ago by
Federico
• 0
4
votes
9
replies
444
views
Faster Needleman-Wunsch rapid global alignment of two sequences?
Needleman-Wunsch
alignment
1 day ago by
Gabriel R.
★ 2.9k
4
votes
2
replies
283
views
GRCh38.gmap file
gnomix
gmap
14 days ago by
lorena9132
▴ 10
4
votes
7
replies
613
views
To get p-values for the TPM
P-value
TPM
RSEM
updated 23 days ago by
dsull
★ 6.0k • written 24 days ago by
VITALA
• 0
4
votes
5
replies
3.4k
views
How to compare compare two Sam files to check mapping
alignment
updated 10 days ago by
DavidStreid
▴ 90 • written 6.4 years ago by
madhu.9124
▴ 60
4
votes
2
replies
276
views
How can I analyze normalized expression data?
DEseq2
RNA-seq
10 days ago by
mnx0723
• 0
3
votes
4
replies
4.0k
views
FarmCPU - how to explain the reported 'effect'?
gwas
updated 10 days ago by
chloek88
• 0 • written 5.6 years ago by
Philipp Bayer
8.5k
3
votes
3
replies
2.5k
views
How to make a TSS enrichment plot in ATAC-seq analysis?
ATAC
updated 23 days ago by
sp
• 0 • written 22 months ago by
Dan
▴ 180
3
votes
5
replies
407
views
Converting CRAM to FastQ
GATK
samtools
cram
SamToFastq
fastq
15 days ago by
Maverick
▴ 10
3
votes
9
replies
629
views
Is it Acceptable to Have Uniform Quality Scores in a FASTQ File?
FASTQ
updated 24 days ago by
Istvan Albert
100k • written 26 days ago by
Κοσμάς
• 0
3
votes
8
replies
692
views
Spike-in control found in raw reads (16S amplicon seq) but not picked up by DADA2 - where to go from here?
nf-core
16S
amplicon
dada2
ampliseq
updated 12 days ago by
Chris Dean
▴ 410 • written 16 days ago by
sovrappensiero
▴ 100
3
votes
5
replies
645
views
SLURM submission problem: Indexing the Reference Genome is not done in STAR
align
RNA-Seq
linux
STAR
26 days ago by
n_navy
• 0
3
votes
5
replies
355
views
Per base sequence content error in RNAseq analysis
RNA-seq
analysis
updated 26 days ago by
GenoMax
142k • written 26 days ago by
ahmad.sajad4541
• 0
3
votes
3
replies
374
views
genome assembly records not present in assembly_summary.txt
ncbi
bacteria
assembly
updated 22 days ago by
GenoMax
142k • written 22 days ago by
sapuizait
▴ 10
3
votes
3
replies
231
views
Getting differential ChIP-seq peaks between conditions after calling consensus peaks
MAnorm
ChIP-seq
consensus
peaks
updated 2 days ago by
ATpoint
82k • written 3 days ago by
Alexandra
• 0
3
votes
1
reply
207
views
Question about methylation location
Methylation
WGBS
bisulfide
updated 8 days ago by
dthorbur
★ 2.0k • written 9 days ago by
Eren
• 0
3
votes
4
replies
755
views
Mapping cDNA sequence of a single gene to a genome not hosted at UCSC server (without Blat)
mapping
26 days ago by
rahu
• 0
3
votes
1
reply
284
views
Differential Expression with limma: Contrast and Design Matrix, combinatorial approach valid?
limma
updated 3 days ago by
dariober
14k • written 5 days ago by
Holly
▴ 30
3
votes
4
replies
326
views
Truncated metadata file report from ENA Portal API
ena
python
8 days ago by
Giulia
• 0
3
votes
3
replies
365
views
Kraken2 database
kraken
microbialdb
database
krakendb
kraken2
updated 5 days ago by
Mathew
▴ 140 • written 8 days ago by
Christopher
• 0
3
votes
3
replies
285
views
what is another word for a BLAST "hit"?
blast
alignment
8 days ago by
dec986
▴ 380
3
votes
3
replies
442
views
absolute path for symbolic links in Snakefile
Snakemake
updated 9 days ago by
Jesse
▴ 770 • written 29 days ago by
yifangt86
▴ 60
3
votes
3
replies
297
views
Getting the nucleotide sequence of proteins, having their UniProt IDs
Nucleotide
Genomic
Sequence
Uniprot
Proteins
updated 26 days ago by
GenoMax
142k • written 26 days ago by
Mariana
▴ 40
3
votes
3
replies
273
views
Genbank vs SRA
ncbi
genbank
genomics
sra
updated 26 days ago by
Mensur Dlakic
★ 27k • written 26 days ago by
c_u
▴ 520
3
votes
6
replies
509
views
install package: package ‘gmwm’ is not available for this version of R
r
updated 6 days ago by
Pine
▴ 20 • written 13 days ago by
snajafy
• 0
3
votes
8
replies
6.6k
views
7 follow
GATK genomicsDBimport intervals for WGS
gatk
genomicsdbimport
updated 16 days ago by
Sd
• 0 • written 5.1 years ago by
Nicolas Rosewick
11k
3
votes
3
replies
381
views
What analysis suitable to identify similarly expressed genes between two samples (treated vs untreated). Contrary to DGE analysis,
Gene-Expression
RNA
NOISeq
DGE
updated 15 days ago by
ATpoint
82k • written 16 days ago by
alifafiq1
• 0
3
votes
0
replies
155
views
News:
Interested in Spatial Omics?
Bioconductor
Spatial-Omics
Spatial-Transcriptomics
updated 25 days ago by
Ram
43k • written 25 days ago by
carlopecoraro2
★ 2.5k
3
votes
5
replies
348
views
Generating mpileup file using samtools
mpileup
samtools
updated 15 days ago by
Joe
21k • written 15 days ago by
Ruqaiya
• 0
3
votes
2
replies
287
views
imputation through beagle
panel
beagle
reference
imputation
4 days ago by
analyst
▴ 50
682 results • Page
2 of 14
Recent Votes
A: How is the design in DESeq2 work?
Error in CIBERSORTx ($ operator is invalid for atomic vectors)
Answer: RNAseq coverage vs depth for transcript isoform expression?
constructing pangenome through psvcp
Differential Expression with limma: Contrast and Design Matrix, combinatorial approach valid?
Differential Expression with limma: Contrast and Design Matrix, combinatorial approach valid?
Answer: RNAseq coverage vs depth for transcript isoform expression?
Recent Locations •
All
Bangladesh,
just now
Chile,
13 minutes ago
USA,
17 minutes ago
United States,
19 minutes ago
Australia,
26 minutes ago
United States,
48 minutes ago
Hong Kong,
48 minutes ago
Recent Awards •
All
Popular Question
to
Muhammad
• 0
Popular Question
to
synat.keam
▴ 100
Scholar
to
jv
★ 1.8k
Popular Question
to
syedahamdani94
• 0
Popular Question
to
mohammadhassanj
▴ 260
Scholar
to
dsull
★ 6.0k
Popular Question
to
finswimmer
16k
Recent Replies
Answer: Checking chromosome builds for genotyping data
by
Muhammad
• 0
Assume you have genotype data in Plink format. (G.bed, G.bim, G.fam) Download some reference panel data in Plink format (R.bed, R.bim, R.f…
Comment: Error in CIBERSORTx ($ operator is invalid for atomic vectors)
by
nguyenn6
• 0
did you ever figure it out? i'm having the same issue.
Comment: Traveler with Infernal mapping failed
by
anton.i.petrov
• 0
Hi Larissa! I am the lead developer of R2DT and I've just noticed this question. Could you please email help@r2dt.bio with your input seque…
Comment: constructing pangenome through psvcp
by
analyst
▴ 50
Fixed the issue by updating nucmer version.
Comment: Blastn error : ncbi::CObject::ThrowNullPointerException() - Attempt to access NU
by
GenoMax
142k
Can you create a small test database (`makeblastdb`) from your query file and try to run the search against the same file and see if that w…
Comment: calculating genomic coverage/ base overlap in R
by
1769mkc
★ 1.2k
you can `dput(head(df)` for the both the data frame so that other can test for possible solutions
Comment: Broad and Narrow peaks
by
ATpoint
82k
What is your question? It's unclear.
Comment: Help with Biopython for Beginner
by
Joe
21k
One question before offering more solutions: are you trying to learn Python with this as an example problem, or are you trying to find the …
Answer: RNAseq coverage vs depth for transcript isoform expression?
by
Gordon Smyth
★ 7.2k
See the exploration of isoform estimation precision vs read length and sequencing depth in our paper: https://doi.org/10.1093/nar/gkad1167.…
Comment: How to handle duplicated genes in TCGA data?
by
txema.heredia
▴ 130
Why does the tool require gene symbols and not ensembl ids? Is it retrieving information from somewhere else? If so, your best bet is to fi…
Comment: how to treat the replicates while performing WGCNA
by
mavy
▴ 10
Thank you so much for your response . Really appreciate it. I will try the way you mentioned and will get back if I have any query
Comment: Blastn error : ncbi::CObject::ThrowNullPointerException() - Attempt to access NU
by
hophuquy0944
• 0
i have the same error, i used high performance computer, here is my code to set memory. srun --nodes=1 --ntasks=1 --cpus-per-task=24 -…
Comment: Overlapping Ranges within Granges object
by
Alex Reynolds
35k
Yes, `bedmap` will perform operations on one or two BED files.
Comment: B allele frequency (BAF)
by
aidangcruickshank
▴ 10
Apologies for resurrecting this post, but any idea what that functions "regions" paramater takes? Would it be a GRanges object? The documen…
Comment: How to handle duplicated genes in TCGA data?
by
Ngrin
• 0
Thanks @txema.heredia.The tool I am going to use only accepts gene symbols. This is the reason. So I cannot use ENS IDs.
Traffic: 1047 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