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119,630 results • Page
5 of 2393
Sort: Rank
Rank
Views
Votes
Replies
0
votes
0
replies
108
views
Mapping gene symbols to MONDO codes
mondo
genes
mapping
12 days ago by
CRivi
• 0
0
votes
0
replies
105
views
Blog:
Tools and Future of eQTL: Data Gathering and Application in Genetic Medicine
eQTL
SNPs
GWAS
12 days ago by
Novogene
▴ 460
1
vote
1
reply
361
views
Strategy to find transgene copy number and integration sites using only Nanopore simplex reads?
sequencing
transgenes
ngs
updated 12 days ago by
colindaven
7.0k • written 16 days ago by
Mark
▴ 20
2
votes
4
replies
286
views
Where can I download a BED file with exonic regions?
exome
bed
updated 11 days ago by
Pierre Lindenbaum
164k • written 12 days ago by
njornet
▴ 20
0
votes
2
replies
273
views
cellranger error - insufficient disc space allocated to cellranger
cellranger
updated 12 days ago by
yura.grabovska
▴ 660 • written 13 days ago by
tony_88888
• 0
0
votes
1
reply
261
views
Pigeon make-seurat produces empty output
isoseq
pigeon
pacbio
updated 11 days ago by
yura.grabovska
▴ 660 • written 13 days ago by
TheCatalyst
• 0
0
votes
2
replies
206
views
How to Process PacBio RS FASTQ Files from SRA for Genome Coassembly with Illumina Reads?
coassembly
fastq
pacbio
updated 12 days ago by
qin
• 0 • written 24 days ago by
till
• 0
0
votes
0
replies
115
views
Germline CNV CALLING
gErmline
CNV
updated 11 days ago by
GenoMax
147k • written 12 days ago by
Smilesky
• 0
0
votes
0
replies
105
views
Packages for constructing Phylogenetic tree from HapMap file
HapMap
tree
Phylogenetic
SNP
12 days ago by
sujee119
• 0
3
votes
5
replies
2.7k
views
How Do I create a BED file from an hard masked fasta?
genome
sequencing
updated 12 days ago by
hewm2008
▴ 50 • written 5.5 years ago by
marcofraca
▴ 20
3
votes
1
reply
343
views
What is the reason that all high throughput sequencing data for the human brain is snRNA-seq instead of scRNA-seq ?
10x
scanpy
python
single-cell
anndata
updated 12 days ago by
jared.andrews07
★ 18k • written 12 days ago by
JACKY
▴ 160
1
vote
2
replies
274
views
Picard LiftoverVCF Maps Variants to Incorrect Chromosomes When Processing Individual Chromosomes
liftovervcf
12 days ago by
jonas.andersson
▴ 40
0
votes
0
replies
113
views
News:
Master Evidence Synthesis with Meta-analysis in R (Online Course - Feb 10-14, 2025)
Meta-analysis
Review
Evidence-Synthesis
12 days ago by
carlopecoraro2
★ 2.6k
0
votes
3
replies
314
views
PCA plot
fviz_pca
factoextra
updated 12 days ago by
Bastien Hervé
5.9k • written 12 days ago by
4732b159
• 0
6
votes
8
replies
866
views
NGS data analysis
NGS
eukaryotic
9 days ago by
Acervo
• 0
0
votes
0
replies
123
views
Intersect between bedGraph and bed file
count
bedtools
bedGraph
Matrix
13 days ago by
daffodil
▴ 10
1
vote
0
replies
372
views
is there any data base or reference to provide a comprehensive list of CD marker expression in different white blood cell types?
DEG
myeloid
CDmarker
leukocyte
13 days ago by
qasemi.m.q
▴ 10
1
vote
2
replies
333
views
How to interpret that overrepresented and duplicate sequences influence %GC content?
Duplicates
FASTQC
MultiQC
Fastq
GC
10 days ago by
tvibhaps
▴ 10
0
votes
0
replies
122
views
Should we normalize/transform WGBS beta values?
normalization
WGBS
methylation
transfromation
13 days ago by
Lalaland
▴ 40
0
votes
4
replies
577
views
What is the best way to confirm if a mutated gene is more frequent in recurrence group than in baseline?
statistics
compare_groups
gene_count
13 days ago by
Lila M
★ 1.3k
0
votes
0
replies
163
views
How to combine replicates in profile plot in profileplyr package?
ATAC-Seq
profilePlot
profilePlyr
updated 13 days ago by
GenoMax
147k • written 14 days ago by
B.N.
▴ 10
0
votes
2
replies
376
views
No Cluster ID's present when making UMAP for Joint RNA and ATAC analysis: Signac 10x multiomic tutorial
multiomics
snATACseq
snRNAseq
14 days ago by
bgbs
• 0
0
votes
0
replies
166
views
Phasing alleles with SHAPEIT4: cases and controls together or separately?
cases-controls
separately
together
case-control
phasing
14 days ago by
igor.alcaras
• 0
2
votes
1
reply
1.8k
views
Is it better to phase two populations together or separately?
phasing
beagle
populations
updated 14 days ago by
igor.alcaras
• 0 • written 9.0 years ago by
eyb
▴ 270
0
votes
3
replies
392
views
Clarification with vcf file
quality
vcf
VCF
score
updated 13 days ago by
GenoMax
147k • written 14 days ago by
Nesma
• 0
2
votes
8
replies
987
views
SRAtoolkit --split-files output
sratoolkit
sra
fastq
14 days ago by
tony_88888
• 0
0
votes
1
reply
282
views
m6A modification prediction using Nanopore DRS data (RNA004)
m6A
DRS
Nanopore
updated 13 days ago by
GenoMax
147k • written 14 days ago by
baibhu1234
• 0
0
votes
0
replies
173
views
database of gmap file for GLIMPSE2 imputation
gmap
GLIMPSE2
14 days ago by
cautree
• 0
3
votes
6
replies
641
views
Create a fasta and gtf file
gtf
human
genome
fasta
updated 14 days ago by
Juke34
8.9k • written 15 days ago by
ATRX
★ 1.1k
1
vote
2
replies
322
views
Regarding to Two-color microarray data analysis (DGE)
Differential-expression-analysis
updated 14 days ago by
Ram
44k • written 15 days ago by
SHIRUI
▴ 10
11
votes
12
replies
1.3k
views
dedup STAR transcriptome file using umi_tools
rna-seq
umi
transcriptome
umi_tools
14 days ago by
ATRX
★ 1.1k
0
votes
1
reply
221
views
ChIP-seq signal values
values
chipseq
signal
updated 15 days ago by
1769mkc
★ 1.2k • written 15 days ago by
SEJAL
• 0
0
votes
0
replies
195
views
Speclib of Rattus novergicus (taxid 10116) to use in DIA-NN
Proteomics
15 days ago by
thalisommoreiraskt
• 0
0
votes
1
reply
281
views
News:
[Survey] Help Shape the Future of Genomic Data Storage Solutions!
genomics
bioinformatics
survey
solutions
storage
updated 15 days ago by
Michael
55k • written 15 days ago by
spacecow
• 0
1
vote
1
reply
279
views
QQ plot with small bump in the middle
QQ-plot.GWAS
updated 14 days ago by
Ram
44k • written 15 days ago by
zhuzhu
▴ 10
4
votes
3
replies
431
views
Confused by reference files
reference
alignment
updated 15 days ago by
GenoMax
147k • written 15 days ago by
Nesma
• 0
3
votes
4
replies
470
views
Contrasts for comparing condition within tissue
limma
deseq2
edgeR
contrasts
updated 14 days ago by
SamGG
▴ 70 • written 15 days ago by
Ben
▴ 20
1
vote
2
replies
380
views
How to Map NCBI taxid to Open Tree of Life ott_id Without Using Scientific Names?
taxonomy
ott
15 days ago by
Martín Ezequiel
• 0
0
votes
2
replies
281
views
Cellranger: Demux pooled (hashing antibodies) GEX and VDJ 10x sequence fastq data
hashing
cellranger
demux
15 days ago by
Flipstone
• 0
11
votes
2
replies
509
views
Tutorial:
Avoiding the Pitfalls of the Anaconda License: A Practical Guide
conda
Anaconda
license
15 days ago by
Juke34
8.9k
0
votes
0
replies
208
views
Fixed peak width in ENCODE TFs ChIP-seq
MACS2
ChIP-seq
ENCODE
15 days ago by
DavideBrex
▴ 20
0
votes
0
replies
213
views
vg call AD frequencies for certain sites
vg
15 days ago by
Danny
• 0
2
votes
2
replies
438
views
Job:
Research Scientist - Bioinformatics position in Milan, Italy
R
Python
RNASeq
singleCell
15 days ago by
kanika.151
▴ 160
0
votes
3
replies
361
views
Questions about finding similar genes and dissimilar genes in BLAST
E-value
similarity
BLAST
updated 15 days ago by
biofalconch
★ 1.3k • written 16 days ago by
William
• 0
1
vote
3
replies
522
views
Question about variant calling method using pangenome-graph
vg
updated 4 days ago by
Jouni Sirén
▴ 470 • written 16 days ago by
Marion
• 0
0
votes
1
reply
276
views
Are there specific pipelines for identifying solo-TIRs?
solo-TIR
elements
transposable
updated 16 days ago by
biofalconch
★ 1.3k • written 16 days ago by
Marcos
▴ 10
3
votes
5
replies
551
views
Optical Duplicates
gatk
MarkDuplicates
optical-duplicates
updated 1 day ago by
Ram
44k • written 16 days ago by
ebogen
▴ 10
4
votes
2
replies
447
views
Tool:
A notebook for checking relatedness and X heterozygosity from sequencing data
heterozygosity
relatedness
sequencing
sex
estimation
16 days ago by
barslmn
★ 2.3k
0
votes
0
replies
230
views
Signac for mgatk scRNA-seq data
mgatk
Signac
scRNA-seq
16 days ago by
marco.barr
▴ 150
0
votes
0
replies
224
views
Homer annotatePeaks.pl output
start
annotatePeaks.pl
chr
homer
position
updated 16 days ago by
GenoMax
147k • written 16 days ago by
Rakesh
• 0
119,630 results • Page
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Comment: Is this featureCounts output normal, and how can I process it for DESeq2 analysi
Answer: Is this featureCounts output normal, and how can I process it for DESeq2 analysi
A: Strandedness Of Homer For Motif Analysis
Comment: database of cancer and normal cell lines
Comment: database of cancer and normal cell lines
How to filter and keep longest isoform per gene in gff3 file ?
A: How To Convert Gencode Gtf Into Bed Format ?
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Recent Replies
Comment: database of cancer and normal cell lines
by
yueli7
▴ 250
Hello GenoMax, Thank you so much for your great help! I really appreciated! Best, Yue
Comment: How to Handle Incorrect Clade Grouping of a Reference Genome in a Phylogenetic T
by
oasiswho
• 0
Dear Mensur Dlakic Thank you very much for your response. I am currently working on constructing a phylogenetic tree based on mitochondrial…
Comment: Detecting genomic signatures of drug resistance breast cancer in transcriptomic
by
DareDevil
★ 4.3k
You can contact me biologsr[at]gmail.com
Answer: How to Handle Incorrect Clade Grouping of a Reference Genome in a Phylogenetic T
by
Mensur Dlakic
★ 28k
> Has anyone experienced a similar issue? I am sure many people have gotten the trees they didn't expect. Assuming you know how to do…
Comment: Is this featureCounts output normal, and how can I process it for DESeq2 analysi
by
Gordon Smyth
★ 7.7k
I can read 50MB files into R in a few seconds on my laptop. Is your R session very short on memory? Anyway, you can undertake a DE analysi…
Comment: Is this featureCounts output normal, and how can I process it for DESeq2 analysi
by
DdogBoss
▴ 20
I will give edgeR a go to see if the resulting feature counts file is easier to handle than in bash. When I try to import the current fea…
Answer: Is this featureCounts output normal, and how can I process it for DESeq2 analysi
by
Gordon Smyth
★ 7.7k
Yes, that is normal output. Have you considered using the simpler R-based interface: ``` library(Rsubread) library(edgeR) files <- c("samp…
Answer: Iterative clustering with silhouette score
by
Mensur Dlakic
★ 28k
You didn't tell us what type of clustering is used here. Specifically, how do you determine the number of clusters? With the information…
Comment: Duplicate ENSGids in the result file quant.genes.sf from Salmon
by
GenoMax
147k
How did you make your `salmon` index? Using the transcript file for v.46 from GENCODE? <!-- this is it -->
Comment: database of cancer and normal cell lines
by
GenoMax
147k
See https://www.proteinatlas.org/humanproteome/cell+line<br> https://gtexportal.org/home/aboutAdultGtex<br> http://gent2.appex.kr/gent2/<b…
Comment: Gene locus and gene ID
by
GenoMax
147k
`ENSG00000260958` is marked as a novel transcript based on [**HAVANA**][1] (manual) analysis. It is overlapping several other items that ar…
Comment: Gene locus and gene ID
by
zizigolu
★ 4.3k
Actually my question is why when IA search for `ENSG00000260958`, these three `TP53TG3GP`, `RARRES2P5` and `FGFR3P5` comes? Does this mean …
Comment: Estimate error-rate and assembly oftion for FLYE assembler
by
GenoMax
147k
If data has been basecalled with `dorado` using super accuracy (SUP) or high accuracy (HAC) models then use the `--nano-hq`.
Comment: Estimate error-rate and assembly oftion for FLYE assembler
by
Umer
▴ 130
Thank you for clerification. based on my Raw data i get error rates around 2–2.2%. Shold i use `--nano-hq` or `--nano-raw`. what do you …
Comment: Rank in rGFA files
by
tsnorri
• 0
Thanks! I’ll check it on Monday.
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