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121,800 results • Page
423 of 2436
Sort: Rank
Rank
Views
Votes
Replies
0
votes
0
replies
608
views
no read counts per allele while using gatk ASEReadCounter
GATK
3.3 years ago by
Sara
▴ 280
1
vote
4
replies
1.5k
views
how to link hmmalign result and FastTree or other Tree tools
FastTree
hmmalign
Phylogenetic_tree
3.3 years ago by
shangguandong1996
▴ 30
0
votes
1
reply
824
views
Distribution of annotated genomic regions in DNAm probes using UCSC_RefGene_Group
DNA
EPIC
R
methylation
updated 3.2 years ago by
Marc
▴ 10 • written 3.3 years ago by
decafcoffeebrewer
• 0
3
votes
6
replies
2.0k
views
Help with PCA plot from SNPRelate
PLOT
SNPRelate
PCA
updated 3.3 years ago by
GenoMax
153k • written 3.3 years ago by
elielsonveloso
• 0
0
votes
0
replies
462
views
WGCNA consensus between RNA seq and microarray datasets
RNA-seq
microarray
WGCNA
3.3 years ago by
Harrsha
• 0
4
votes
2
replies
2.6k
views
correct list of capture targets/intervals for SureSelect mouse exome to perform GATK Mutect2
mouse exom
Mutect2
list of intervals
pon
updated 3.3 years ago by
heskett
▴ 110 • written 5.8 years ago by
ati_
▴ 40
0
votes
1
reply
2.0k
views
Infinium MethylationEPIC Annotation under hg38
Microarray
Methylation
3.3 years ago by
Molin
▴ 10
1
vote
1
reply
1.6k
views
Illumina EPIC array manifest file header
EPICarray
Illumina
updated 3.3 years ago by
Molin
▴ 10 • written 3.6 years ago by
현호
• 0
0
votes
2
replies
1.3k
views
Third Quartile (Q3) for RNAseq data
normalization
RNAseq
Third
Q3
R
3.3 years ago by
Leo
• 0
1
vote
2
replies
2.0k
views
Admixture: "PLINK Input file error"
plink
admixture
3.2 years ago by
dec986
▴ 380
0
votes
0
replies
889
views
Job:
Staff Data Scientist, Computational Biology
learning
immunology
cardiovascular
drug
machine
biology
discovery
Computational
3.3 years ago by
arajan
• 0
2
votes
2
replies
816
views
Build canine dna.primary_assembly.fa for kb ref
bustools
Ensembl
kallisto
updated 2.2 years ago by
Ram
45k • written 3.3 years ago by
Candice
• 0
1
vote
2
replies
2.4k
views
What is Nanopore Barcode Score and how is it calculated?
barcoding
nanopore
demultiplexing
DNA-Seq
updated 3.3 years ago by
andres.firrincieli
3.9k • written 3.5 years ago by
dedeoglumbg
▴ 10
0
votes
0
replies
455
views
Standard for aligning smallRNA to a reference human rRNA?
rRNA
RNAseq
miRNA
3.3 years ago by
Mauro
▴ 20
0
votes
0
replies
562
views
Help with mounting VCF file parameters adenovo
denovo
stacks
snp
vcf
asembly
3.3 years ago by
Pamella
• 0
2
votes
5
replies
2.5k
views
Giotto Error: py_run_file_impl(file, local, convert) : ModuleNotFoundError: No module named 'dataclasses'
Giotto
ModuleNotFoundError
3.2 years ago by
Agatha Nabilla L
▴ 10
4
votes
4
replies
1.4k
views
Renaming reads
fastq
rename
sed
UMI
3.2 years ago by
vvs.hazia
▴ 10
0
votes
2
replies
1.3k
views
User error in GATK CreateSomaticPanelOfNormals
gatk
CreateSomaticPanelOfNormals
user-error
3.2 years ago by
Hasib
▴ 20
0
votes
0
replies
443
views
Drawing multiple genes and adding possibile functional sites (from Clover)?
gviz
ensembl
r
clover
biomart
3.3 years ago by
Ale
• 0
11
votes
8
replies
12k
views
7 follow
Working with GTEX dataset
GTEX
RNA-Seq
updated 2.7 years ago by
Ram
45k • written 10.2 years ago by
pbio
▴ 150
0
votes
1
reply
905
views
Integrate scRNAseq with 10x Multiome
10x
Multiome
updated 3.3 years ago by
mikhael.manurung
▴ 50 • written 3.3 years ago by
fmazzio1
▴ 10
1
vote
1
reply
789
views
Looking for Bulk RNA seq PBMC data
rba
genome
rna-seq
updated 3.2 years ago by
Ram
45k • written 3.3 years ago by
Emily
▴ 70
0
votes
4
replies
1.3k
views
FASTA sequence retrieval
FASTA
Genes
DEGs
3.2 years ago by
Roy.anupama11
• 0
0
votes
1
reply
3.1k
views
How to use NCBI API key for Entrez (Biopython)?
NCBI
Entrez
updated 3.3 years ago by
vkkodali_ncbi
★ 3.9k • written 3.3 years ago by
William
• 0
5
votes
5
replies
14k
views
How to get number of characters (nucleotides) in fasta file
count
fasta
linux
characters
commands
updated 3.3 years ago by
bio_driven
• 0 • written 4.2 years ago by
er.doug.ragnar
▴ 30
2
votes
4
replies
1.6k
views
Htseq-count: Problem with feature counts
gtf
RNA-Seq
htseq-count
updated 3.3 years ago by
Istvan Albert
103k • written 3.3 years ago by
MolGeek
▴ 80
0
votes
1
reply
584
views
identification of agilent micro array non coding RNA id
micro
id
conversion
array
updated 3.3 years ago by
GenoMax
153k • written 3.3 years ago by
Dr. Pradeep
• 0
10
votes
10
replies
4.2k
views
6 follow
Rna Seq Analysis Script
Next-Gen-Sequencing
Script
Ubuntu
bash
RNA-Seq
3.3 years ago by
SomeOne
▴ 240
0
votes
0
replies
953
views
Job:
ML researcher - Oxford-GSK Institute for Molecular and Computational Medicine (IMCM) in data analysis and integration in neurodegenerative disease
learning
integration
Machine
IMCM
neurodegeneration
analysis
3.3 years ago by
SH01
• 0
1
vote
1
reply
1.2k
views
Gene enrichment analysis R studio error
RStudio
updated 3.3 years ago by
Thomas
▴ 10 • written 3.6 years ago by
iamsmor
• 0
0
votes
1
reply
562
views
Morbidity inheritance dataset
inheritance
Morbidity
updated 3.3 years ago by
Michael
56k • written 3.3 years ago by
ManuelDB
▴ 110
1
vote
1
reply
875
views
What is a biologically meaningful size of gene module?
module
gene
updated 3.3 years ago by
andres.firrincieli
3.9k • written 3.3 years ago by
druggable
▴ 60
0
votes
0
replies
488
views
Immediate segmentation error when using STAR on SMART-Seq data
segmentation
smart-seq
dumped
scRNA-seq
STAR
3.3 years ago by
Bertalan_Takacs
▴ 140
0
votes
1
reply
719
views
Genome Fasta and compatible tss region database
igv
tss
fasta
tata
box
updated 3.3 years ago by
dthorbur
★ 3.0k • written 3.3 years ago by
Luca
• 0
0
votes
2
replies
976
views
bwa error
index
bwa
updated 2.4 years ago by
Ram
45k • written 3.3 years ago by
amahdi779
• 0
2
votes
2
replies
1.0k
views
CNV analysis
DELLY
CNV
wholegenomesequencing
S.pombe
3.3 years ago by
archanaverma433
▴ 10
0
votes
2
replies
871
views
Can a pathogenic mutation results in the up-regulation of a gene?
mutation-up-regulation
Pathogenic
3.3 years ago by
nazaninhoseinkhan
▴ 530
0
votes
3
replies
1.4k
views
DESeq2 use of factors for colData
DESeq2
expression
differential
updated 3.3 years ago by
swbarnes2
15k • written 3.3 years ago by
mcsimenc
▴ 30
2
votes
2
replies
1.2k
views
How to provide read1 and read2 fastq files from two lanes to kallisto | bustools?
kallisto
10X
bustools
scRNA-seq
3.3 years ago by
eager_underdog
• 0
11
votes
5
replies
9.4k
views
6 follow
How to make a summary plot like below?
cancer
classes
Oncoplots
updated 3.3 years ago by
Thind amarinder
▴ 340 • written 4.2 years ago by
Jianlan
▴ 10
3
votes
4
replies
1.7k
views
snakemake r script
pipeline
snakemake
3.3 years ago by
nishimalhotra2612
▴ 50
0
votes
10
replies
2.6k
views
Reassembly after Binning
binning
3.2 years ago by
Tanker
• 0
0
votes
0
replies
529
views
extract utr 5' from refGene.txt
genes
utr
igv
3.3 years ago by
Luca
• 0
1
vote
8
replies
2.6k
views
AttributeError: 'int' object has no attribute 'seq'
BioPython
AttributeError
3.2 years ago by
Robert
• 0
6
votes
6
replies
7.2k
views
How to remove rRNA, bacterial RNA and polyA contamination from RNA-seq data(fastq format)?
RNA-Seq
sequencing
updated 3.3 years ago by
Dreamer
▴ 40 • written 8.2 years ago by
Megan
▴ 50
19
votes
8
replies
23k
views
7 follow
rRNA Removal In Rna-Seq Data
rna-seq
deseq
updated 2.7 years ago by
Trinh
▴ 10 • written 11.8 years ago by
jockbanan
▴ 440
29
votes
18
replies
28k
views
9 follow
Cleaning RNA-Seq data from rRNA
RNA-Seq
rRNA cleaning
QC
updated 3.3 years ago by
Dreamer
▴ 40 • written 9.4 years ago by
debitboro
▴ 270
16
votes
7
replies
8.3k
views
6 follow
rRNA decontamination of RNA-Seq reads (tool choice, introns etc)
rRNA
intron
RNA-Seq
bbsuite
sormeRNA
updated 2.5 years ago by
GenoMax
153k • written 5.8 years ago by
Anand Rao
▴ 640
8
votes
10
replies
10k
views
8 follow
rRNA remove from RNAseq data
RNA-Seq
updated 3.3 years ago by
Dreamer
▴ 40 • written 7.1 years ago by
Peter
▴ 40
1
vote
4
replies
1.2k
views
Tool:
Quick Command to Filter Bam Files
bed
awk
3.3 years ago by
Sasha
▴ 850
121,800 results • Page
423 of 2436
Recent Votes
Answer: How to obtain a refFlat file for the Rat
Answer: mummer4: how do I get the mapview executable?
Comment: RTG (Real Time Genomics) docker image - Problem dealing with different VCFs
Answer: GSEA vs GO enrichment
Answer: How to account for solvent controls in DESeq2 when comparing follicular vs lutea
A: fgsea: What does fgseaMultilevel argument sampleSize mean/when to change it?
A: fgsea: What does fgseaMultilevel argument sampleSize mean/when to change it?
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Answer: Local Synteny Analysis with Uncharacterized Genes
by
Philipp Bayer
8.8k
For gene clusters of this smaller size I'd recommend [clinker](https://github.com/gamcil/clinker) There are some nice automated visualisat…
Comment: Samtools flagstat
by
Istvan Albert
103k
It is an interesting point that I have not considered. I looked up the SAM specification, it states: For secondary alignments: "*One of …
Comment: Local Synteny Analysis with Uncharacterized Genes
by
GenoMax
153k
Prior thread with some tools: https://www.biostars.org/p/9477510/ `SynTracker` described in: https://www.nature.com/articles/s41587-024-02…
Comment: mummer4: how do I get the mapview executable?
by
GenoMax
153k
As long as the output is in the right format mapview should work with v.4.x. You will need to compile it from older release.
Comment: How to detect divergent domains in AlphaFold models (CDD/InterProscan not workin
by
LLG
• 0
Thank you very much, I'll try those!
Comment: mummer4: how do I get the mapview executable?
by
Tospohh
▴ 10
oh, good catch, I didn't see that. That's a shame. The output in the examples looks very useful. Since there isn't any detail about the rea…
Answer: mummer4: how do I get the mapview executable?
by
GenoMax
153k
`mapview` program is deemed obsolete in v.4.x (see https://github.com/mummer4/mummer/blob/master/OBSOLETE.md ). You may need to compile it …
Comment: How to obtain a refFlat file for the Rat
by
GenoMax
153k
> but nothing work What does not work? Once you export a file from the link included, it is in refFlat format.
Comment: RTG (Real Time Genomics) docker image - Problem dealing with different VCFs
by
stuckinanendlessfebruary
• 0
Thanks for replying! Yes, the DRAGEN VCF (dragen_HG008.norm.vcf.gz) is indeed multi-sample, containing both HG008-N (Normal) and HG008-T-m…
Comment: RTG (Real Time Genomics) docker image - Problem dealing with different VCFs
by
Jeremy Leipzig
23k
which columns are giving you trouble? is the problem that you have two samples in dragen (tumor/normal) and only one sample in the hg008?
Comment: How to obtain a refFlat file for the Rat
by
AIMAR
▴ 70
I've try the mentioned methods but nothing work that's why I've asked again If I can find a new solution. Thanks !
Answer: How to obtain a refFlat file for the Rat
by
GenoMax
153k
Please don't ask the same question again in a new thread. This was answered a few weeks back: https://www.biostars.org/p/9613666/#9613671 …
Answer: Is a direct comparison of the number of up- and down-regulated genes meaningful?
by
benformatics
4.1k
Usually it is not very useful. The only situation where it makes sense to use is where you do a gradient treatment (e.g. 0M, 5M, 50M, et…
Answer: Is a direct comparison of the number of up- and down-regulated genes meaningful?
by
ATpoint
89k
No, don't rely on numbers. This can and is strongly influences by the sample size and noise, and by this power. Even at same sample size it…
Comment: Pseudobulk analysis using AggregateExpression()
by
adhisadi
• 0
Hi, Did you figure this out? In my data some gene expressed in very low number of cells (less than 1% of total cells) appear as differentia…
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