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122,200 results • Page
627 of 2444
Sort: Rank
Rank
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Votes
Replies
1
vote
4
replies
2.6k
views
How to view if a gene is protein-coding?
genetics
protein-coding
genes
updated 4.4 years ago by
fracarb8
★ 1.8k • written 4.4 years ago by
DN99
▴ 20
2
votes
6
replies
2.2k
views
IMPUTE2 minimal number of SNPs per chunk
impute
gwas
updated 4.4 years ago by
LauferVA
4.8k • written 4.4 years ago by
nhaus
▴ 420
0
votes
1
reply
990
views
IMPUTE2 limit to only one population of 1000G Reference
GWAS
impute
1000g
updated 4.4 years ago by
LauferVA
4.8k • written 4.4 years ago by
nhaus
▴ 420
1
vote
3
replies
1.5k
views
SortSam Error after BWA alignment
alignment
mappingquality
picard
sortsam
bwa
4.3 years ago by
loy_loy
▴ 10
2
votes
12
replies
8.3k
views
Confused with 2 SRA runs for one sample
runs
Illumina
RNASeq
sra
4.4 years ago by
ConfusedSheep
▴ 10
0
votes
2
replies
1.6k
views
Unicycler error not enough memory available
assembly
unicycler
memory
updated 4.4 years ago by
Mensur Dlakic
★ 30k • written 4.4 years ago by
A_heath
▴ 180
0
votes
3
replies
4.7k
views
PubChem CID in ChEMBL
ChEMBL
PubChem
updated 4.4 years ago by
a.kalashnikov
• 0 • written 6.6 years ago by
jpsangio
• 0
0
votes
2
replies
987
views
DESeq2 no replicates analysis with a design value of ~1 generates only positive log2foldchange
DESeq2
Log2FoldChange
4.4 years ago by
BIN
• 0
0
votes
6
replies
1.8k
views
extracting only one sex from gnomad genome v.3.1 file
gnomad
4.4 years ago by
storm1907
▴ 30
4
votes
0
replies
947
views
Herald:
The Biostar Herald for Friday, July 02, 2021
herald
updated 4.4 years ago by
natay
20 • written 4.4 years ago by
Biostar
3.7k
1
vote
7
replies
16k
views
hisat2-align exited with value 1
alignment
RNA-Seq
rna-seq
updated 4.4 years ago by
27shym
• 0 • written 6.7 years ago by
m.t.lorenc
• 0
1
vote
4
replies
1.3k
views
Pseudocode for gapped BLAST seed extension
Pseudocode
smith-waterman
seed
extend
BLAST
updated 4.4 years ago by
GenoMax
154k • written 4.4 years ago by
Daniel
▴ 10
6
votes
4
replies
1.6k
views
RNA-seq normalisation
normalisation
RNAseq
4.4 years ago by
raavi21198
▴ 20
0
votes
0
replies
534
views
Calculate of Total Hip BMD
Hip
BMD
4.4 years ago by
Yong
▴ 10
1
vote
1
reply
1.0k
views
Identify the potential TF involved in the regulation of DEGs
Transcription
factors
gene
list
R
updated 4.4 years ago by
Zhilong Jia
★ 2.2k • written 4.4 years ago by
ryme
▴ 30
0
votes
0
replies
778
views
Job:
Postdoctoral Associate in statistical geneticist . Nantes/France
france
nantes
postdoc
4.4 years ago by
Pierre Lindenbaum
166k
0
votes
1
reply
1.1k
views
Rarefy metagenomic adatasets for taxonomic profiling using MetaPhlAn3
metagenomics
Rarefy
MetaPhaln3
Genomics
updated 4.4 years ago by
andres.firrincieli
3.9k • written 4.4 years ago by
serene.s
• 0
1
vote
3
replies
1.4k
views
Calculates the percent sequenceCalculates the percent sequence identity for a pairwise sequence alignment
pairwise
sequence
alignment
identity
updated 3.9 years ago by
Jeremy Leipzig
23k • written 4.4 years ago by
Emy Alade
▴ 40
0
votes
1
reply
1.0k
views
High-throughput sequence variant analysis: Using BAM or VCF files?
ICGC
VCF
BAM
High-throughput
updated 4.4 years ago by
ATpoint
90k • written 4.4 years ago by
Zahra
▴ 110
2
votes
4
replies
1.9k
views
Subsetting fastq file based on reads starting with a specific pattern
fastq
subset
4.4 years ago by
biomon
▴ 60
2
votes
5
replies
3.2k
views
Visualizing the gene network obtained by WGCNA
WGCNA
weighted
network
visualizing
4.4 years ago by
seta
★ 1.9k
4
votes
7
replies
4.4k
views
How to move the files from sub folder and sub-sub folders into one other folder?
bash
updated 2.7 years ago by
Ram
45k • written 4.4 years ago by
mathavanbioinfo
▴ 80
0
votes
0
replies
1.0k
views
Where to find GATK4 ACNV
segmentation
CNV
ABSOLUTE
GATK
4.4 years ago by
noona
• 0
3
votes
5
replies
1.8k
views
Integration of two TCGA datasets
r
RNA-Seq
tcga
survival
updated 4.4 years ago by
Kevin Blighe
★ 90k • written 4.4 years ago by
fifty_fifty
▴ 90
3
votes
4
replies
2.4k
views
Generating Positional List from VCF
guidance
updated 2.1 years ago by
Thind amarinder
▴ 340 • written 4.4 years ago by
Ared445
▴ 60
3
votes
6
replies
2.4k
views
KentUtils Installation Problem
kenutils
gff3ToGenePred
gff3
UCSC
gff
4.4 years ago by
mglasena
▴ 40
3
votes
3
replies
2.7k
views
DESeq2 saying that dimensions of count matrix and metadata don't agree, but they do agree
expression
R
differential
4.4 years ago by
hippo
▴ 10
7
votes
8
replies
7.1k
views
Aligning PacBio hifiasm CCS to reference genome using pbmm2
assembly
pbmm2
pacbio
hifiasm
updated 3.6 years ago by
gconcepcion
▴ 410 • written 4.5 years ago by
K
▴ 10
4
votes
6
replies
2.5k
views
How to find out TFBS motifs within 5'-UTR sequences
5prime-UTR
TFBSmotifs
updated 16 months ago by
Ram
45k • written 4.4 years ago by
isha.lily20
▴ 10
1
vote
1
reply
883
views
Ways to mapping a transcriptome against a single gene
annotation
RNAseq
updated 4.4 years ago by
dsull
★ 7.8k • written 4.4 years ago by
arturo.marin
▴ 20
3
votes
3
replies
6.3k
views
How to plot phylogenetic tree using R packages
ape
phylogenetic
ggtree
4.4 years ago by
Kumar
▴ 170
1
vote
3
replies
1.5k
views
Identify unique genes and protein families from eukaryotic genome
Phylogenetic
SNP
Unique
tree
gene
updated 4.4 years ago by
Dunois
★ 2.9k • written 4.4 years ago by
nazninislamnif
▴ 20
11
votes
13
replies
3.0k
views
6 follow
Bioinformatics
tag1
tag2
updated 4.4 years ago by
Joe
22k • written 4.4 years ago by
m90
▴ 30
0
votes
0
replies
716
views
How to resolve Basic4cseq package printwigfile function error
NGS
R
4Cseq
DNAseq
4.4 years ago by
koushikayaluri
▴ 70
0
votes
0
replies
858
views
Small sample sizes in dapc, adegenet.
find.clusters
clusters
adegenet
populations
dapc
4.4 years ago by
Ismaelrymy
• 0
2
votes
1
reply
838
views
Forum:
Is there a way to look into funding proposals of published papers?
funding
updated 4.4 years ago by
Mensur Dlakic
★ 30k • written 4.4 years ago by
ilante
▴ 30
0
votes
1
reply
1.3k
views
minimap2 aligning sequencing reads to barcodes
demultiplex
nanopore
sequencing
minimap2
updated 4.4 years ago by
GenoMax
154k • written 4.4 years ago by
matthew.tarnowski1
• 0
1
vote
1
reply
1.1k
views
Multiple identical mutations in SnpEff result: ex1.genes.txt
mutation
SnpEff
updated 4.4 years ago by
Ram
45k • written 4.4 years ago by
Maya
• 0
1
vote
1
reply
1.4k
views
Deseq DEG genes to Cytoscape for network visualization?
deseq
cytoscape
deg
updated 4.4 years ago by
YanO
▴ 140 • written 4.4 years ago by
manekineko
▴ 10
0
votes
2
replies
1.1k
views
Script for cascade molecular dynamics
cascading
script
moleculardynamics
4.4 years ago by
Samilla
• 0
1
vote
2
replies
1.6k
views
filter VCF by HGVS - indel normalisation
VCF
VEP
updated 4.4 years ago by
Emily
24k • written 4.4 years ago by
michal.inbar
• 0
2
votes
4
replies
1.8k
views
BLAST Database error: No alias or index file found for nucleotide database
blast
blastx
updated 4.4 years ago by
GenoMax
154k • written 4.4 years ago by
langziv
▴ 70
1
vote
1
reply
1.5k
views
Job:
Bioinformatics Scientist in the department of Research Technology at Tufts University
scRNASeq
Python
R
genomics
updated 4.4 years ago by
francis
▴ 280 • written 4.4 years ago by
Rebecca
• 0
2
votes
2
replies
3.8k
views
How to set a multiqc outpath
fastqc
multiqc
4.4 years ago by
michael.flower.14
▴ 210
0
votes
0
replies
1.5k
views
logistic Principal Component Analysis for binary data (gene presence absence between 3 states)
gene
logistic
PCA
binary
4.4 years ago by
Jonathan Yoou
▴ 70
1
vote
6
replies
2.0k
views
How to use DELLY on Galaxy
DELLY
Galaxy
updated 4.4 years ago by
benformatics
4.2k • written 4.4 years ago by
ritiksinha005
▴ 10
0
votes
0
replies
774
views
Visualising SeqRecords with compound locations
genbank
snapgene
benchling
biopython
4.4 years ago by
timothy.kirkwood
▴ 140
0
votes
0
replies
759
views
how to get a consensus sequence for each sample in a vcf file using a reference sequence?
vcf
fasta
sequence
updated 2.5 years ago by
Ram
45k • written 4.4 years ago by
daniellamodukpe
• 0
0
votes
0
replies
948
views
maxT permutation in plink
plink
gwas
4.4 years ago by
nhaus
▴ 420
2
votes
1
reply
1.4k
views
Using OrthoMCL on command line
orthomcl
updated 4.4 years ago by
dariober
15k • written 4.4 years ago by
DNAlias
▴ 40
122,200 results • Page
627 of 2444
Recent Votes
Answer: Can i use orthofinder for small protein datasets and not full proteome?
Comment: Can i use orthofinder for small protein datasets and not full proteome?
Answer: Can i use orthofinder for small protein datasets and not full proteome?
Answer: Can i use orthofinder for small protein datasets and not full proteome?
Answer: Midpoint rooting IQTREE newick file moves node support around
Answer: Subsetting before QC in Spatial Transcriptomics
Answer: Feature Counts vs Salmon quantification
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Teacher
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dthorbur
★ 3.2k
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to
colindaven
8.1k
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ATpoint
90k
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san96
▴ 190
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Wilber0x
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Recent Replies
Comment: Can i use orthofinder for small protein datasets and not full proteome?
by
alexandrakortsi
• 0
By sequence. Thank you for your response!
Comment: Why did the QV value decrease significantly after using YAHS for HiC scaffolding
by
xinguok794
▴ 10
Thank you for your reply! Unfortunately, despite running YAHS with `--no-contig-ec`, the QV value of the resulting FASTA file did not impro…
Comment: Subsetting before QC in Spatial Transcriptomics
by
Kent
▴ 30
Hi Kevin, Thanks for the detailed explanation. Due to the characteristics of the datasets, we initially used very lenient quality control…
Comment: Midpoint rooting IQTREE newick file moves node support around
by
Luca Arbore
▴ 10
Thank you very much Kevin, it worked!
Comment: ID unifiying across different datasets
by
GenoMax
154k
In this case the entry notes that this is likely the product of a pseudogene: https://www.uniprot.org/uniprotkb/Q5VTE0/entry and existence …
Comment: Comparison of different RNAseq data sets
by
DrSmad
▴ 10
Each lab contributes both control and LPS. Example, for cell line A_lab1 did and analysis on control and LPS-6h. Cell line B_lab2 did contr…
Comment: ID unifiying across different datasets
by
zizigolu
★ 4.4k
sorry, why some gene names are often lacking though the Uniprot ID is still valid (using biomart)?
Comment: snpEff: Unsupported structural variant types
by
shpak.max
▴ 70
Unfortunately, while it ran without a problem initially, when I checked the run screen today, I saw the following error message (and unlike…
Comment: ID unifiying across different datasets
by
GenoMax
154k
You can use the [**ID mapping tool**][1] from UniProt site (third ID did not map from the list above): From To P68104 ENSG0000015…
Answer: The geo samples is not having sentrix id and sentrix position. But this informat
by
yura.grabovska
▴ 890
Crosspost from related question: https://www.biostars.org/p/9616466/#9616534 ``` ##Using R, illuminaio from Bioconductor library(…
Answer: Finding Sentrix ID in HM450K arrays
by
yura.grabovska
▴ 890
``` ##Using R, illuminaio from Bioconductor library(illuminaio) temp.idat <- readIDAT(file = "200379120087_R02C02_Grn.idat") tem…
Comment: Can i use orthofinder for small protein datasets and not full proteome?
by
michael.ante
★ 4.0k
Do you want to compare them by sequence or by function? For the later, you can use e.g. InterProScan, KoFamScan.
Answer: Can i use orthofinder for small protein datasets and not full proteome?
by
dthorbur
★ 3.2k
If you're just using the tool for clustering purposes, I think OrthoFinder might be a little clunky and would recommend using something lik…
Comment: ID unifiying across different datasets
by
zizigolu
★ 4.4k
Thank you; The problem is let's say in the protein ID column I see `Q5VTE0;P68104;Q05639` here I am sure I should get which `ENSG` for eac…
Comment: How to improving 2-Nucleotide RNA-seq Mapping Accuracy
by
2411110159
• 0
Since we do not have real data yet, I tried to simulate this using strand-specific RNA bisulfite-seq reads (C to T). Read1 corresponds to t…
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