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121,054 results • Page
1 of 2422
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0
votes
0
replies
35
views
pLoF variants for gnomAD v.4
gnomAD
pLoF
variants
grch38
4 hours ago by
Damianos P. Melidis
▴ 40
2
votes
4
replies
228
views
No variant in the Pseudoautosomal regions of gomad chrY ?
chrY
PAR
vcf
gnomad
Pseudoautosomal
1 hour ago by
Pierre Lindenbaum
166k
0
votes
1
reply
84
views
Genomic Data Portal (GDC) download a given a link file
GDC
R
TCGA
TCGAbiolinks
maftools
7 hours ago by
bioinformagician
• 0
836
votes
167
replies
174k
views
111 follow
News:
The Biostar Handbook. A bioinformatics e-book for beginners.
training
handbook
updated 14 days ago by
Biostar
3.5k • written 8.4 years ago by
Istvan Albert
102k
0
votes
4
replies
136
views
How to generate identiy score between aligned sequences with Mauve?
identity
score
alignment
mauve
6 hours ago by
marongiu.luigi
▴ 740
5
votes
7
replies
2.3k
views
6 follow
Cluster annotation in single cell
Single-cell
updated 22 hours ago by
Shiyang
• 0 • written 19 months ago by
synat.keam
▴ 100
0
votes
1
reply
154
views
Finding matched RNA-seq and Ribo-seq datasets for Nicotiana benthamiana under the same condition
rna-seq
ribo-seq
translation-efficiency
dataset-search
nicotiana-benthamiana
updated 1 day ago by
colindaven
7.4k • written 1 day ago by
Farshid
• 0
0
votes
4
replies
406
views
Limma model gives weird results
model
multivariate
Limma
updated 1 day ago by
SamGG
▴ 90 • written 4 days ago by
leranwangcs
▴ 150
3
votes
4
replies
423
views
How to download the entire C. elegans genome from WormBase into Excel with automated gene descriptions
Gene
Wormbase
Celegans
updated 1 day ago by
GenoMax
151k • written 2 days ago by
bioinformatics_rk
▴ 10
0
votes
0
replies
127
views
Job:
Postdoctoral Research Fellow, multi-omics, Univ of Nebraska Medical Center, Omaha, NE, USA
microbiome
Postdoc
metagenome
transcriptome
metabolome
updated 2 days ago by
GenoMax
151k • written 2 days ago by
era
• 0
0
votes
0
replies
131
views
How to deal with the clusterProfiler analysis result?
clusterProfiler
updated 2 days ago by
GenoMax
151k • written 2 days ago by
Tundup
• 0
0
votes
0
replies
148
views
News:
Genome Bioinformatics Summer School: OMICSS-25
training
bioinformatics
school
2 days ago by
Lilit
• 0
1
vote
2
replies
223
views
Unable to find mitochondrial genes in latest rat genome(GRCr8)
seurat
genome
mitochondrialgenes
NCBI
Singlecell
2 days ago by
dxj294
• 0
0
votes
0
replies
117
views
Haplotype reference for ShapeIt (ShapeIt5)
Phasing
2 days ago by
evan.kransdorf
• 0
6
votes
6
replies
322
views
Pre-Made STAR Index for mm10 Mouse Genome
STAR
updated 1 day ago by
colindaven
7.4k • written 2 days ago by
Nerelys
• 0
1
vote
1
reply
183
views
The volcano plot shows data with an arm-shaped enrichment.
volcanoplot
updated 2 days ago by
ATpoint
87k • written 2 days ago by
lea.preuss
• 0
0
votes
0
replies
138
views
Tool:
GENetLib: A Python Library for Gene–environment Interaction Analysis via Deep Learning
gene-environment
interaction
analysis
2 days ago by
Barry
• 0
9
votes
10
replies
492
views
STAR vs. Kallisto
STAR
kallisto
alignment
RNA-Seq
mapping
updated 2 days ago by
dsull
★ 7.4k • written 2 days ago by
gogeni5529
▴ 70
0
votes
0
replies
122
views
How to Annotate VCF with AlphaMissense Using VEP and dbNSFP v5.1a in Offline Mode?
AlphaMissense
dbNSFP
VEP
ensembl
2 days ago by
DareDevil
★ 4.4k
1
vote
1
reply
213
views
News:
Phylogenetic Comparative Methods in R (12–16 May, Online)
R
Phylogenetic-Comparative-Methods
updated 2 days ago by
Meeru
▴ 10 • written 3 days ago by
Physalia-courses
★ 2.6k
0
votes
1
reply
196
views
Biostar handbook
Handbook
Biostar
updated 2 days ago by
GenoMax
151k • written 2 days ago by
himanshu0102
• 0
2
votes
2
replies
1.4k
views
pangenome - Create a diagram venn
roary
grep
awk
pangenome
venn
updated 3 days ago by
mplace
▴ 40 • written 2.0 years ago by
BATMAN
• 0
4
votes
4
replies
313
views
Addressing two nuisance factors in RNAseq
bulkRNAseq
updated 2 days ago by
ATpoint
87k • written 3 days ago by
jkim
▴ 190
1
vote
5
replies
346
views
DRAGEN FILTER
dragen
variant-calling
updated 3 days ago by
GenoMax
151k • written 3 days ago by
theresia.celine
▴ 10
0
votes
1
reply
312
views
Interpretation of the results: PCA
proteomics
PCA
updated 1 day ago by
rfran010
★ 1.4k • written 3 days ago by
Ariadna
▴ 20
3
votes
5
replies
370
views
How to check normal BAM_files before create a Panel Of Normals (PoN)
GATK
variant_calling
PoN
3 days ago by
AIMAR
• 0
0
votes
1
reply
240
views
how to handle infinite M-values in methylation array data
M-value
methylation
infinite
array
updated 3 days ago by
Basti
★ 2.1k • written 4 days ago by
matt192
• 0
1
vote
3
replies
1.8k
views
Free and redistributable genomic data sets?
data
software-development
genomics
updated 3 days ago by
Meeru
▴ 10 • written 9.2 years ago by
woemler
▴ 170
2
votes
5
replies
1.2k
views
Rna-seq data
data
rna-seq
updated 3 days ago by
GenoMax
151k • written 3.2 years ago by
biology_inform
▴ 60
6
votes
3
replies
1000
views
RNAseq example data
expression
RNA-Seq
data
next-gen
updated 3 days ago by
ehaag
▴ 20 • written 4.6 years ago by
rakinitopo
▴ 10
0
votes
1
reply
334
views
Transcript_id with "-0" after "flair collapse"
flair
updated 3 days ago by
GenoMax
151k • written 5 months ago by
anna_shin
• 0
0
votes
0
replies
179
views
Can I use glucose measured using two different devices in my study?
normalization
standardization
transformation
3 days ago by
Faith
▴ 50
1
vote
3
replies
727
views
Snakemake - pipeline shut down without error
snakemake
4 days ago by
bhumm
▴ 200
3
votes
2
replies
305
views
Source for `transcript_name` in GTFs
GTF
updated 3 days ago by
Jorge - Ensembl
▴ 30 • written 4 days ago by
gernophil
▴ 120
5
votes
5
replies
706
views
Tool:
Lightweight bash pipeline for ddRADseq read pre-processing, demultiplexing, and de-duplication using cutadapt
rad-seq
ddRADseq
demultiplexing
deduplication
4 days ago by
Rafal
▴ 10
0
votes
2
replies
242
views
How to normalised DNA sequencing depth for genomic variant discovery ?
normalisation
read-depth
variant-calling
updated 4 days ago by
Ram
45k • written 4 days ago by
AIMAR
• 0
2
votes
4
replies
348
views
RNASeq featureCounts Help Needed
fungi
featurecounts
RNASeq
4 days ago by
SomeOne
▴ 170
0
votes
0
replies
191
views
PAUP* error with exporting result file
PAUP
SVDquartet
4 days ago by
ylkim9
• 0
0
votes
1
reply
218
views
I need to convert Axiom output to PLINK format I did not find annotation.db
Axiom
PLINK
apt-format-result
updated 4 days ago by
GenoMax
151k • written 4 days ago by
AlmuhayyaA
• 0
1
vote
3
replies
349
views
How to merge heterogeneously normalized RNA-seq datasets for meta-analysis?
normalization
rna-seq
updated 3 days ago by
ATpoint
87k • written 4 days ago by
pipelinfections
• 0
1
vote
1
reply
295
views
Tool:
I packaged some tools in python pypi for Windows (fastqc, bowtie2, samtools)
python
pypi
updated 1 day ago by
Dunois
★ 2.9k • written 4 days ago by
Cris
▴ 10
0
votes
3
replies
394
views
Transcript ID
id
transcript
updated 4 days ago by
Meeru
▴ 10 • written 5 days ago by
cheong
• 0
0
votes
1
reply
265
views
Galaxy + RStudio
R
RNA-seq
RStudio
updated 4 days ago by
swbarnes2
14k • written 4 days ago by
justus
• 0
8
votes
18
replies
3.2k
views
8 follow
How to limit fasta header to 40 characters?
unix
seqkit
fasta
updated 4 days ago by
jena
▴ 320 • written 20 months ago by
fishingline37
• 0
1
vote
2
replies
332
views
Transcript level quantification and gene length scaling for rRNA depleted libraries
RNASeq
updated 5 days ago by
dsull
★ 7.4k • written 5 days ago by
marc.zimmerli
▴ 10
0
votes
0
replies
232
views
Model diagnostics for GAM (Generalised Additive Model)
gam
mgcv
generalized-additive-model
5 days ago by
Tuấn Anh
• 0
2
votes
5
replies
741
views
Forum:
Small‑Lab Data Management & Analytics Tool – What are your biggest pain points?
biotech
startup
updated 5 days ago by
Darked89
4.7k • written 8 days ago by
Novoo
▴ 10
1
vote
1
reply
297
views
landscape of RNA types and their functions/ scRNA
transcriptomics
scRNA
biology
updated 5 days ago by
ATpoint
87k • written 5 days ago by
Ariadna
▴ 20
1
vote
5
replies
485
views
Is vg toolkit suitable for haplotype calling?
pangenome
haplotype
vg
updated 1 day ago by
Jordan M Eizenga
▴ 700 • written 5 days ago by
Pau
• 0
0
votes
0
replies
220
views
Dfam annotations
dfam
5 days ago by
frarodmar17
• 0
121,054 results • Page
1 of 2422
Recent Votes
DRAGEN FILTER
C: theta value and R value in SNP data
C: theta value and R value in SNP data
theta value and R value in SNP data
Answer: No variant in the Pseudoautosomal regions of gomad chrY ?
Answer: Phylogenetic Comparative Methods in R (12–16 May, Online)
No variant in the Pseudoautosomal regions of gomad chrY ?
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151k
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Comment: No variant in the Pseudoautosomal regions of gomad chrY ?
by
Pierre Lindenbaum
166k
Ah, somehow your answer is right, in the reference the PAR on chrY is masked: $ samtools faidx red.fasta "chrY:10001-2781479" | tail …
Comment: How to extract specific chromosome from vcf file
by
Reza
• 0
Perhaps something like this is more compact: vcftools --gzvcf <file.vcf.gz> $( seq -f "--chr %g" 1 23 ) --recode --out subset_chr1-23
Comment: No variant in the Pseudoautosomal regions of gomad chrY ?
by
GenoMax
151k
Will delete then. See if you get any good answers directly. Most of the papers that GPT used as source appear to be older (~ mid-2000s).
Comment: No variant in the Pseudoautosomal regions of gomad chrY ?
by
Pierre Lindenbaum
166k
@genomax yeah, I asked GPT too but I don't think it's right (?). The reads are mapped using bwa so even if the regions are similar between…
Answer: No variant in the Pseudoautosomal regions of gomad chrY ?
by
GenoMax
151k
GPT says the following. Until we get an answer this seems logical. There *are* actually variants in the pseudoautosomal regions (PARs) of …
Comment: How to generate identiy score between aligned sequences with Mauve?
by
marongiu.luigi
▴ 740
Thank you, I used `[skani][1]` but it requires the build a model of several genomes together. Can I use it for only two genomes? [1]: …
Comment: How to generate identiy score between aligned sequences with Mauve?
by
marongiu.luigi
▴ 740
Thank you, I ran with `progressiveMauve --weight=15 --output=./out_file.mauve chr1.fa` where `chr1.fa` is a multifasta with the two genomes…
Answer: Genomic Data Portal (GDC) download a given a link file
by
bioinformagician
• 0
Solved using this, then merging all maf files into one. But would like a solution to download that one in specific just to check if it is t…
Comment: How to generate identiy score between aligned sequences with Mauve?
by
GenoMax
151k
According to the manual a file is supposed to be produced by Mauve: https://darlinglab.org/mauve/user-guide/files.html#:~:text=The%20identi…
Answer: How to generate identiy score between aligned sequences with Mauve?
by
GenoMax
151k
`FastANI` has bee recommended by users here for this type of comparison (since you are mentioning `Mauve` you are likely referring to genom…
Comment: Cosmic database update issue in annovar
by
Ahmed
• 0
Ensure that the cosmic input files are not compressed. Also, Try using following prepare_annovar_user.pl: `http://www.openbioinformatics.o…
Answer: Cluster annotation in single cell
by
Shiyang
• 0
I'd like to recommend a new tool called **mLLMCelltype** that can greatly simplify the cluster annotation process for single-cell RNA-seq d…
Comment: Interpretation of the results: PCA
by
rfran010
★ 1.4k
I would say exact interpretations depend more on the nature of the data, experimental setup, and data processing steps. You provided some g…
Answer: Finding matched RNA-seq and Ribo-seq datasets for Nicotiana benthamiana under th
by
colindaven
7.4k
This might be very tricky. Try here https://sra-explorer.info/ Search for: ("Nicotiana benthamiana"[Organism] OR Nicotiana bent…
Comment: Pre-Made STAR Index for mm10 Mouse Genome
by
colindaven
7.4k
HiSat is another RNA-seq aligner which uses less RAM.
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