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121,800 results • Page
618 of 2436
Sort: Rank
Rank
Views
Votes
Replies
2
votes
3
replies
1.3k
views
How can download and read BAM and FASTQ format
fastq
miseq
BAM
updated 4.2 years ago by
swbarnes2
15k • written 4.2 years ago by
bahaddin
• 0
1
vote
3
replies
2.2k
views
log2 normalization produces NaNs
r
updated 2.7 years ago by
Ram
45k • written 4.2 years ago by
melissachua90
▴ 70
0
votes
1
reply
1.2k
views
RnBeads Greedycut command ???
greedycut
rnbeads
array
methylation
updated 4.2 years ago by
almsu798
• 0 • written 4.9 years ago by
Ankit
▴ 520
0
votes
3
replies
1.1k
views
Phylogeny Analysis tools
Phylogeny
updated 4.2 years ago by
Dunois
★ 2.9k • written 4.2 years ago by
nazninislamnif
▴ 20
0
votes
3
replies
1.1k
views
how can I get alignment quality from bam index file?
NGS
samtools
galaxy
updated 2.2 years ago by
Ram
45k • written 4.2 years ago by
microorganism_001
▴ 30
2
votes
5
replies
1.8k
views
Issue installing Plink
Plink
4.2 years ago by
AndrMod
• 0
3
votes
2
replies
1.0k
views
Suggestions for an undergraduate research project on glioblastoma
glioblastoma
Python
Cancer
R
updated 4.1 years ago by
Ram
45k • written 4.2 years ago by
Caitlin
▴ 100
7
votes
7
replies
9.8k
views
Mummer To Viewable Alignment Format (Fasta Or Aln...)
genomics
alignment
updated 4.2 years ago by
krinsman
• 0 • written 14.0 years ago by
Yannick Wurm
★ 2.5k
0
votes
0
replies
1.0k
views
how to get effect sizes (R2) in result of GEMMA?
GEMMA
SNP
updated 2.4 years ago by
Ram
45k • written 4.2 years ago by
Kumar
▴ 170
0
votes
0
replies
592
views
miRNA to families
python
families
RNAseq
miRNA
R
4.2 years ago by
ehruan
▴ 10
2
votes
7
replies
2.3k
views
Good QC Package (RSeQC or alternative) for Salmon mapping/quantification results?
RSeQC
Salmon
RNA-Seq
mapping
updated 4 months ago by
squidqid
• 0 • written 4.2 years ago by
skjw1029
▴ 80
3
votes
0
replies
3.4k
views
Why does the Seurat FindMarkers function report different log fold change values than the FoldChange function?
single
scRNA-seq
cell
RNA-Seq
Seurat
4.2 years ago by
imdoingascience
▴ 40
0
votes
1
reply
1.9k
views
High levels of duplicated reads Illumina from PCR-free libraries
fastqc
PCR
duplicate
reads
Illumina
updated 4.2 years ago by
GenoMax
153k • written 4.2 years ago by
grey
▴ 40
12
votes
5
replies
1.6k
views
how to sort the rows of a file as a matrix?
linux
updated 23 months ago by
Ram
45k • written 4.2 years ago by
BATMAN
• 0
2
votes
2
replies
1.8k
views
WGCNA - GTEx RNASeq - Help choosing a soft power
WGCNA
RNA-Seq
GTEx
4.2 years ago by
Branden
• 0
0
votes
0
replies
448
views
How to deal with fractional number for enrichment analysis
protein
analysis
enrichment
4.2 years ago by
Cancan
• 0
0
votes
2
replies
1.9k
views
Normalization/Scaling with sctransform in RStudio of scRNASeq data
vst
normalization
sctransform
scRNASeq
scaling
4.2 years ago by
ConfusedSheep
▴ 10
1
vote
4
replies
2.4k
views
How to view if a gene is protein-coding?
genetics
protein-coding
genes
updated 4.2 years ago by
fracarb8
★ 1.7k • written 4.2 years ago by
DN99
▴ 20
2
votes
6
replies
2.0k
views
IMPUTE2 minimal number of SNPs per chunk
impute
gwas
updated 4.2 years ago by
LauferVA
4.8k • written 4.2 years ago by
nhaus
▴ 420
0
votes
1
reply
893
views
IMPUTE2 limit to only one population of 1000G Reference
GWAS
impute
1000g
updated 4.2 years ago by
LauferVA
4.8k • written 4.2 years ago by
nhaus
▴ 420
1
vote
3
replies
1.4k
views
SortSam Error after BWA alignment
alignment
mappingquality
picard
sortsam
bwa
4.1 years ago by
loy_loy
▴ 10
2
votes
12
replies
7.4k
views
Confused with 2 SRA runs for one sample
runs
Illumina
RNASeq
sra
4.2 years ago by
ConfusedSheep
▴ 10
0
votes
2
replies
1.5k
views
Unicycler error not enough memory available
assembly
unicycler
memory
updated 4.2 years ago by
Mensur Dlakic
★ 29k • written 4.2 years ago by
A_heath
▴ 170
0
votes
3
replies
4.2k
views
PubChem CID in ChEMBL
ChEMBL
PubChem
updated 4.2 years ago by
a.kalashnikov
• 0 • written 6.4 years ago by
jpsangio
• 0
0
votes
2
replies
893
views
DESeq2 no replicates analysis with a design value of ~1 generates only positive log2foldchange
DESeq2
Log2FoldChange
4.2 years ago by
BIN
• 0
0
votes
6
replies
1.7k
views
extracting only one sex from gnomad genome v.3.1 file
gnomad
4.2 years ago by
storm1907
▴ 30
4
votes
0
replies
876
views
Herald:
The Biostar Herald for Friday, July 02, 2021
herald
updated 4.2 years ago by
natay
20 • written 4.2 years ago by
Biostar
3.6k
1
vote
7
replies
16k
views
hisat2-align exited with value 1
alignment
RNA-Seq
rna-seq
updated 4.2 years ago by
27shym
• 0 • written 6.5 years ago by
m.t.lorenc
• 0
1
vote
4
replies
1.2k
views
Pseudocode for gapped BLAST seed extension
Pseudocode
smith-waterman
seed
extend
BLAST
updated 4.2 years ago by
GenoMax
153k • written 4.2 years ago by
Daniel
▴ 10
6
votes
4
replies
1.5k
views
RNA-seq normalisation
normalisation
RNAseq
4.2 years ago by
raavi21198
▴ 20
0
votes
0
replies
488
views
Calculate of Total Hip BMD
Hip
BMD
4.2 years ago by
Yong
▴ 10
1
vote
1
reply
893
views
Identify the potential TF involved in the regulation of DEGs
Transcription
factors
gene
list
R
updated 4.2 years ago by
Zhilong Jia
★ 2.2k • written 4.2 years ago by
ryme
▴ 30
0
votes
0
replies
740
views
Job:
Postdoctoral Associate in statistical geneticist . Nantes/France
france
nantes
postdoc
4.2 years ago by
Pierre Lindenbaum
166k
0
votes
1
reply
965
views
Rarefy metagenomic adatasets for taxonomic profiling using MetaPhlAn3
metagenomics
Rarefy
MetaPhaln3
Genomics
updated 4.2 years ago by
andres.firrincieli
3.9k • written 4.2 years ago by
serene.s
• 0
1
vote
3
replies
1.2k
views
Calculates the percent sequenceCalculates the percent sequence identity for a pairwise sequence alignment
pairwise
sequence
alignment
identity
updated 3.7 years ago by
Jeremy Leipzig
23k • written 4.2 years ago by
Emy Alade
▴ 20
0
votes
1
reply
924
views
High-throughput sequence variant analysis: Using BAM or VCF files?
ICGC
VCF
BAM
High-throughput
updated 4.2 years ago by
ATpoint
89k • written 4.2 years ago by
Zahra
▴ 110
2
votes
4
replies
1.7k
views
Subsetting fastq file based on reads starting with a specific pattern
fastq
subset
4.2 years ago by
biomon
▴ 60
2
votes
5
replies
3.0k
views
Visualizing the gene network obtained by WGCNA
WGCNA
weighted
network
visualizing
4.2 years ago by
seta
★ 1.9k
4
votes
7
replies
4.2k
views
How to move the files from sub folder and sub-sub folders into one other folder?
bash
updated 2.4 years ago by
Ram
45k • written 4.2 years ago by
mathavanbioinfo
▴ 80
0
votes
0
replies
946
views
Where to find GATK4 ACNV
segmentation
CNV
ABSOLUTE
GATK
4.2 years ago by
noona
• 0
3
votes
5
replies
1.6k
views
Integration of two TCGA datasets
r
RNA-Seq
tcga
survival
updated 4.2 years ago by
Kevin Blighe
89k • written 4.2 years ago by
fifty_fifty
▴ 90
3
votes
4
replies
2.1k
views
Generating Positional List from VCF
guidance
updated 22 months ago by
Thind amarinder
▴ 340 • written 4.2 years ago by
Ared445
▴ 60
3
votes
6
replies
2.2k
views
KentUtils Installation Problem
kenutils
gff3ToGenePred
gff3
UCSC
gff
4.2 years ago by
mglasena
▴ 40
3
votes
3
replies
2.5k
views
DESeq2 saying that dimensions of count matrix and metadata don't agree, but they do agree
expression
R
differential
4.2 years ago by
hippo
▴ 10
7
votes
8
replies
6.3k
views
Aligning PacBio hifiasm CCS to reference genome using pbmm2
assembly
pbmm2
pacbio
hifiasm
updated 3.4 years ago by
gconcepcion
▴ 410 • written 4.3 years ago by
K
▴ 10
4
votes
6
replies
2.2k
views
How to find out TFBS motifs within 5'-UTR sequences
5prime-UTR
TFBSmotifs
updated 13 months ago by
Ram
45k • written 4.2 years ago by
isha.lily20
▴ 10
1
vote
1
reply
795
views
Ways to mapping a transcriptome against a single gene
annotation
RNAseq
updated 4.2 years ago by
dsull
★ 7.6k • written 4.2 years ago by
arturo.marin
▴ 20
3
votes
3
replies
6.0k
views
How to plot phylogenetic tree using R packages
ape
phylogenetic
ggtree
4.2 years ago by
Kumar
▴ 170
1
vote
3
replies
1.4k
views
Identify unique genes and protein families from eukaryotic genome
Phylogenetic
SNP
Unique
tree
gene
updated 4.2 years ago by
Dunois
★ 2.9k • written 4.2 years ago by
nazninislamnif
▴ 20
11
votes
13
replies
2.8k
views
6 follow
Bioinformatics
tag1
tag2
updated 4.2 years ago by
Joe
22k • written 4.2 years ago by
m90
▴ 30
121,800 results • Page
618 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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