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542 results • Page
2 of 11
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Votes
Replies
0
votes
0
replies
197
views
Copy number variation plot
Copy-number-variation
genomics
updated 4 days ago by
Ram
43k • written 4 days ago by
Emmi
• 0
0
votes
0
replies
170
views
SNP calling with ANGSD and ngsLD. How many SNPs?
lcwgs
ngsTools
ANGSD
genomics
4 days ago by
DanielEB_fisk
▴ 20
0
votes
1
reply
271
views
Could you please assist in identifying this cluster?
single-cell
updated 4 days ago by
Ram
43k • written 4 days ago by
Kazo
• 0
0
votes
0
replies
190
views
Conversion to tree format
PLINK
bed
Figtree
SplitsTree
updated 4 days ago by
Ram
43k • written 4 days ago by
Dinmukhamed
• 0
0
votes
0
replies
188
views
miRDeep2: How to get the read counts
mirdeep2
4 days ago by
Atul K.
• 0
0
votes
0
replies
196
views
Lncipedia GTF file error
Proteomics
updated 4 days ago by
Ram
43k • written 4 days ago by
atharvakarkare14
▴ 10
3
votes
3
replies
452
views
Free/open source 23andme-like analysis
SNPs
genomics
NGS
VCF
updated 3 days ago by
swbarnes2
14k • written 4 days ago by
joe
▴ 510
0
votes
2
replies
525
views
How to get the reference panel for UKBB
UKBB
GWAS
clump
4 days ago by
航太郎
• 0
0
votes
0
replies
207
views
create genewise sync file in popoolation
popoolation
updated 4 days ago by
GenoMax
141k • written 4 days ago by
N.Y.Wiyana-Hewage
• 0
0
votes
2
replies
362
views
error in coding potential calculator CPC2
cpc
CPC2
coding-potential
4 days ago by
Ashok
• 0
0
votes
2
replies
403
views
miRNAs quantification using mirdeep2 tool
differential-expression
mirdeep2
miRNA
4 days ago by
Ashok
• 0
0
votes
0
replies
207
views
Variant Generation Using Longshot
long-reads
variant-calling
ONT
minion
longshot
updated 5 days ago by
Ram
43k • written 5 days ago by
samuelkalandarov2002
▴ 10
0
votes
2
replies
413
views
QC exclusion of A/T or G/C alleles to avoid strand issues
quality-control
SNV
QC
SNP
4 days ago by
_quantum_girl_
▴ 10
0
votes
0
replies
197
views
traying to make a maf from an already annotated vcf
vcf
vcf2maf
maf
maftools
VEP
1 day ago by
Javier
• 0
0
votes
0
replies
172
views
Pruning with plink finds a majority of SNPs in very high LD
LD
SNP
plink
pruning
5 days ago by
enferdeflame
• 0
1
vote
1
reply
402
views
Difference when using difference number of pathways score to compare between 3 groups
GSVA
Limma
updated 2 days ago by
Gordon Smyth
★ 7.0k • written 5 days ago by
Chris
▴ 260
0
votes
1
reply
397
views
How to add rowLinks, rowTree in SummarizedExperiment manually.
phylogenetic-tree
microbiome
updated 5 days ago by
Ram
43k • written 19 months ago by
Muhammad
• 0
0
votes
0
replies
155
views
How can I obtain the tissue or sample name alongside the Tau score in tspex?
tau-score
tspex
updated 5 days ago by
Ram
43k • written 5 days ago by
bioinfo223
▴ 10
0
votes
0
replies
170
views
How to root an unrooted tree with a known root tree?
phylogenetics
rooting
R
5 days ago by
P.
• 0
0
votes
0
replies
163
views
Issues with SnpEff Assuming Circular Chromosomes in Eukaryotic Genome Analysis
snpEff
5 days ago by
ekirsch
• 0
1
vote
1
reply
372
views
Load a full GFF3 into annotation track using arrow (Apollo)
arrow
python-apollo
Apollo
3 days ago by
renan.igor
• 0
0
votes
0
replies
166
views
filter the most significant ligand and receptors in netVisual_bubble in cell chat
cellchat
5 days ago by
synat.keam
▴ 100
0
votes
1
reply
259
views
assembly using CCS, CLR, CCS_CLR sequences together?
assembly
updated 5 days ago by
GenoMax
141k • written 5 days ago by
ycts
• 0
0
votes
4
replies
567
views
Per base sequence content failed miserably
fastqc
sequence
trimmomatic
NGS
assembly
4 days ago by
Kai Xin
• 0
1
vote
1
reply
218
views
Retrieve a % coverage for each transcript
RNA-seq
updated 5 days ago by
Ram
43k • written 5 days ago by
jammydodger123456
▴ 40
0
votes
2
replies
361
views
How can I solve this error?
metal
5 days ago by
22211020193
• 0
0
votes
0
replies
161
views
Struggling to lift genome builds
PLINK
liftover
GWAS
updated 5 days ago by
GenoMax
141k • written 6 days ago by
srimmer
• 0
1
vote
2
replies
264
views
Can I readmap short reads to rDNA references?
rDNA
assembly
updated 5 days ago by
Ram
43k • written 6 days ago by
aniigodwinn
• 0
0
votes
0
replies
349
views
Looking for an explanation as to what the Peak Score is from HOMER, not finding any answers on Biostars yet
Homer
ATAC-seq
6 days ago by
Ronin
• 0
2
votes
7
replies
794
views
Removing duplicates
duplicates
ONT
minimap2
updated 4 days ago by
joe
▴ 510 • written 6 days ago by
quentinperriere
• 0
0
votes
1
reply
191
views
Annotating a dataset with gnomAD v4 using Hail
Python
Sequencing
Hail
Exome
Annotation
updated 6 days ago by
DKA
▴ 40 • written 6 days ago by
james.melhorn
• 0
0
votes
1
reply
177
views
Freyja plot error
Freyja
updated 6 days ago by
Ram
43k • written 6 days ago by
Adyasha
• 0
0
votes
0
replies
152
views
BIOM format can contain tabular data ?
BIOM
phyloseq
biomformat
R
6 days ago by
chemokine-1
▴ 10
0
votes
4
replies
486
views
How to reduce the variation of CIBERSORTx results?
CIBERSORTx
deconcolution
5 days ago by
feather-W
• 0
0
votes
2
replies
209
views
Bedmethyl file format
bedmethyl
methylation
updated 6 days ago by
GenoMax
141k • written 6 days ago by
njornet
▴ 20
0
votes
0
replies
164
views
sequence table for DADA2 chimera filtering
OTU
sequencetable
DADA2
6 days ago by
Ali
• 0
2
votes
4
replies
303
views
SnpEff annotates coding duplication as intronic?
snpeff
6 days ago by
kirill.zaslavsky
• 0
0
votes
2
replies
235
views
Calculating percentage of cells proliferating in single cell rna seq data
statistics
scRNA-seq
proliferation
6 days ago by
mropri
▴ 150
0
votes
0
replies
138
views
Input into WGCNA and Error on constructNetworks on RNA-Seq data - unique rownames
rownames
RNA-Seq
WGCNA
unique
6 days ago by
shasabhi1
• 0
0
votes
0
replies
127
views
How to summarize dbCAN3 results
dbCAN
CAZy
CAZyme
dbCAN3
dbCAN2
6 days ago by
Nishat
• 0
0
votes
0
replies
150
views
what exactly is a k-mer table (remora)?
remora
basecall
6 days ago by
anne
• 0
1
vote
1
reply
170
views
Help/Direction Needed for Data Analysis of RNA
Sequencing
RNA-seq
DNA-Seq
updated 6 days ago by
dsull
★ 5.8k • written 6 days ago by
niruf
• 0
0
votes
0
replies
136
views
GWAS Phenotypes
GWAS
7 days ago by
solomoncharles77
▴ 90
0
votes
2
replies
300
views
GSEA analysis in R
GSEA
R
Arabidopsis
5 days ago by
Sudip
• 0
0
votes
0
replies
119
views
Add geno header to VariantAnnotation objects
nichenet
scRNA-seq
7 days ago by
QX
• 0
2
votes
5
replies
418
views
Where to find the homopolymer regions bed file for Hg002 genome?
simple-repeats
hg002
bed
homopolymer-regions
6 days ago by
Bikram Kumar
• 0
0
votes
2
replies
249
views
Statistical Advice Needed for RNAseq Data Analysis
Statistical-Significance
Genomics
RNA-seq
Data-Analysis
updated 7 days ago by
Ram
43k • written 7 days ago by
David
• 0
1
vote
2
replies
258
views
Can I compare kallisto counts from samples with different amount of reads?
RNA-seq
kallisto
6 days ago by
bioinfo
▴ 150
0
votes
1
reply
184
views
How to get the reference panel sites for TOPMed hg37 and 38
Imputation
updated 7 days ago by
bk11
★ 2.3k • written 7 days ago by
sinhas
• 0
0
votes
1
reply
199
views
merging Seurat objects after SCT
Seurat
SCT
updated 7 days ago by
Ram
43k • written 7 days ago by
michelle.swarovski
• 0
542 results • Page
2 of 11
Recent Votes
Comment: Redirection of Duplicate PMIDs
Comment: Failed kmer content
Using vg gamsort with naive sorting algorithm
Answer: Using vg gamsort with naive sorting algorithm
Interested in Spatial Omics?
Interested in Spatial Omics?
Comment: Downsampling fastq file
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Recent Awards •
All
Popular Question
to
Kash
▴ 110
Scholar
to
GenoMax
141k
Scholar
to
anovak
▴ 120
Popular Question
to
pfee418
▴ 10
Popular Question
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sarahmanderni
▴ 100
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Michael
54k
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michael.flower.14
▴ 180
Recent Replies
Comment: Subset Seurat object from Xenium spatial data
by
bk11
★ 2.3k
For subsetting a sample, you can do something like this- Idents(seuratObj) <- "orig.ident" subj1 <- c("subject_1") subj1_seur…
Comment: Redirection of Duplicate PMIDs
by
LauferVA
4.2k
Ok! I have a recommendation. I'll submit it as an answer, pending your feedback. vincent
Comment: DYH17 Structure Prediction
by
anasjamshed
▴ 120
In modeller we need to use templates as well.so 63% is acceptable
Comment: DYH17 Structure Prediction
by
Ram
43k
Mensur said > The latter option assumes you know how to use Modeller Do you know how to use Modeller? I vaguely recall there being a mini…
Comment: Should I remove unlocalized scaffols in reference genome before alignment?
by
GenoMax
141k
OP is working with long reads so the chances of reads aligning to unlocalized scaffolds are relatively small. Doing some testing may be suf…
Comment: What is the real meaning of relative enrichment/peak height of ChIP-seq tracks?
by
ATpoint
81k
I personally think that comparing the same peak between conditions is meaningful and comparing peaks within the same sample is not.
Comment: Should I remove unlocalized scaffols in reference genome before alignment?
by
ATpoint
81k
These regions are present in the genome and removing them might incorrectly redirect alignments to known genes. I don't see why you would r…
Comment: Should I remove unlocalized scaffols in reference genome before alignment?
by
njornet
▴ 20
Ok thank you! Do you know if there is an easy way of doing so with ncbi-genome-download or I need to use another tool?
Comment: Using vg gamsort with naive sorting algorithm
by
Pierre Lindenbaum
161k
> Don't forget to follow up on your threads. If an answer was helpful, you should upvote it; if the answer resolved your question, you shou…
Comment: Redirection of Duplicate PMIDs
by
dominickd
• 0
The scope is all publications related to grants from an NIH award program. There are currently ~120k publications in total (about a few hun…
Answer: Using vg gamsort with naive sorting algorithm
by
anovak
▴ 120
The `-d` sorting mode does the entire sort in memory, so it will only work if you have enough memory to load your whole GAM file. To fin…
Comment: Redirection of Duplicate PMIDs
by
dominickd
• 0
I have a list of PMIDs for publications linked to a list of grants, exported from NIH RePORTER.
Comment: Plot DNA methylation level of DMR on the basis of certain genes
by
Pierre Lindenbaum
161k
> Don't forget to follow up on your threads. If an answer was helpful, you should upvote it; if the answer resolved your question, you shou…
Comment: Should I remove unlocalized scaffols in reference genome before alignment?
by
GenoMax
141k
Yes you can remove those if you are only interested in annotated genes.
Comment: Help for coding: Trinity for differential gene expression studies
by
mchour
• 0
[This could help][1] [1]: https://github.com/trinityrnaseq/RNASeq_Trinity_Tuxedo_Workshop/wiki/Trinity-De-novo-Transcriptome-Assembly-W…
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