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121,919 results • Page
712 of 2439
Sort: Rank
Rank
Views
Votes
Replies
3
votes
6
replies
3.4k
views
User-defined coverage in CollectHsMetrics [Picard]
next-gen
picard
coverage
broadinstitute
updated 4.6 years ago by
sh001
• 0 • written 8.2 years ago by
anu014
▴ 190
3
votes
14
replies
3.7k
views
Samtools depth to get the read depth
sequencing
RNA-Seq
4.6 years ago by
bandanaschapagain
▴ 40
4
votes
4
replies
7.2k
views
How to get real cell names from Seurat Object?
rna-seq
updated 4.6 years ago by
from the mountains
▴ 250 • written 4.6 years ago by
leranwangcs
▴ 150
0
votes
0
replies
777
views
Is there a way to identify which MSTRGs (novel StringTie transcripts) are potential novel ncRNAs?
MSTRG
RNAseq
StringTIe
ncRNA
Novel Transcripts
4.6 years ago by
Jen
▴ 100
7
votes
23
replies
8.1k
views
Batch download genome feature file by RefSeq
gbff
ncbi
refseq
4.6 years ago by
ben83
▴ 50
3
votes
3
replies
4.6k
views
How to download a list of all KEGG orthologs with respect to KEGG module (or pathway) in Python?
kegg
database
python
updated 3.2 years ago by
Alexander
• 0 • written 4.6 years ago by
O.rka
▴ 750
3
votes
2
replies
1.8k
views
How to check for completeness of a mitochondrial or chloroplast genome?
genome-completeness
organelles
updated 24 months ago by
Ram
45k • written 4.6 years ago by
kristina.mahan
▴ 170
0
votes
2
replies
1.9k
views
minimap2 alignment for maker
maker
minimap2
annotation
alignment
4.6 years ago by
gilsorek12
▴ 10
0
votes
0
replies
673
views
How can I analyze a VCF dataset without an annotated reference genome
RNA-Seq
R
genome
gatk
galaxy
4.6 years ago by
julianneradford
▴ 20
2
votes
6
replies
4.8k
views
convert DNA FASTA file to RNA FASTA file
RNA-Seq
ChIP-Seq
sequence
updated 4.6 years ago by
JC
13k • written 4.6 years ago by
xiaoleiusc
▴ 140
0
votes
0
replies
588
views
Centrifuge (Classifier for metagenomic sequences)
software error
4.6 years ago by
amanpruthi15
• 0
0
votes
3
replies
2.1k
views
How can I run "gene set enrichment" (not necessarily GSEA) with only one condition?
metagenomics
gene set enrichment
analysis
GSEA
4.6 years ago by
O.rka
▴ 750
0
votes
0
replies
635
views
smallRNA-seq alignment with bowtie1:what is the argument for handling multi-mapped reads?
alignment
smallRNA-seq
bowtie1
multi-mapped reads
updated 4.6 years ago by
GenoMax
153k • written 4.6 years ago by
ooluwayiose
• 0
1
vote
1
reply
1.6k
views
tsv file genome coverage
tsv
genome
updated 4.6 years ago by
Biostar
20 • written 4.6 years ago by
kimkes25
▴ 50
0
votes
8
replies
1.9k
views
Finding suboptimal alignments
sequencing
DNA
alignment
updated 4.6 years ago by
Mensur Dlakic
★ 30k • written 4.6 years ago by
trinityduke100
▴ 10
13
votes
11
replies
6.1k
views
8 follow
Visualization of protein structure in R (Shiny)
R
rshiny
pdb
protein structure
visualization
updated 4.5 years ago by
n.s.j.vandervelden
▴ 90 • written 5.0 years ago by
aquaq
▴ 40
0
votes
1
reply
2.2k
views
Convert .sqn file to .gbk
organelle
updated 24 months ago by
Ram
45k • written 4.6 years ago by
kristina.mahan
▴ 170
1
vote
3
replies
2.5k
views
PCA with PLINK and SmartPCA: same imput file but different results in my plot. Why?
PCA
PLINK
smartPCA
EIGENSTRAT
plot
4.6 years ago by
francesca94.minnai
• 0
3
votes
1
reply
1.7k
views
Tool for extracting copy number alterations from a .maf mutation file
cna
maf
updated 4.6 years ago by
Kevin Blighe
89k • written 4.6 years ago by
genomics Newbie
▴ 90
1
vote
4
replies
1.6k
views
Change sample order in plotHeatmap?
deepTools
plotHeatmap
computeMatrix
updated 3.1 years ago by
Alice Laigle
• 0 • written 4.6 years ago by
konsta.kukkonen
• 0
3
votes
5
replies
3.0k
views
Clustering sequences with low identity
clustering
sequences
updated 4.6 years ago by
Mensur Dlakic
★ 30k • written 4.6 years ago by
agata88
▴ 870
0
votes
1
reply
742
views
ICGC data download
ICGC
local server
4.6 years ago by
Zahra
▴ 110
0
votes
1
reply
784
views
how to make BBmerge produce same strand fastq file
BBmerge
4.6 years ago by
shangguandong1996
▴ 30
3
votes
5
replies
2.1k
views
Newbie CIGAR question
SNP
alignment
sequence
updated 4.6 years ago by
Biostar
20 • written 8.9 years ago by
michael
• 0
1
vote
0
replies
1.4k
views
How to get RSIDs of indels from GWAS summary statistics
R
gene
snp
4.6 years ago by
Fede_Santos95
▴ 20
2
votes
2
replies
943
views
VCF keep only genotyped positions
vcf
genotype
snp
4.6 years ago by
sahahig469
▴ 10
0
votes
2
replies
894
views
compare a list of RNA with RNA sequence in RFAM using python
RNA-Seq
RFam
Python
4.6 years ago by
phangou10
• 0
0
votes
0
replies
586
views
Duplicates probability depending on the number of flow cells
next-gen
sequencing
duplicates
4.6 years ago by
kseniya.petrova
• 0
0
votes
7
replies
1.6k
views
deseq2 design with two variables
deseq2
design
4.6 years ago by
biosjm
• 0
2
votes
1
reply
996
views
Is OMA suitable for prediction of GO function in metagenomic datasets?
OMA
GO_Label
updated 4.6 years ago by
clement.train
▴ 60 • written 4.8 years ago by
crl111222
▴ 10
0
votes
4
replies
1.4k
views
Oligo algorithm analyzer
oligo analyzer
primer
4.6 years ago by
anasofiamoreira94
▴ 80
2
votes
3
replies
1.3k
views
How to convert gff3 format, PASApipeline
RNA-Seq
Assembly
updated 4.6 years ago by
Juke34
9.3k • written 4.6 years ago by
Ruixuan
• 0
1
vote
11
replies
2.2k
views
ground truth dataset for BAM read counts
genome
alignment
read counts
ground truth
4.6 years ago by
Marius
▴ 30
1
vote
1
reply
1.0k
views
Splice junction coordinates for Ensembl transcripts
Ensembl
Splicing
Annotation
updated 4.6 years ago by
Emily
24k • written 4.6 years ago by
AJ_S
• 0
8
votes
3
replies
1.5k
views
how to select features for high dimension data?
machine-learning
updated 22 months ago by
Ram
45k • written 4.6 years ago by
pt.taklifi
▴ 70
16
votes
10
replies
8.2k
views
from txt to bed
ChIP-Seq
updated 4.6 years ago by
Biostar
20 • written 8.5 years ago by
dimitrischat
▴ 210
0
votes
0
replies
396
views
Mitochondrial genome sequence
sequencing
4.6 years ago by
ganesh_swamy2005
• 0
3
votes
9
replies
3.7k
views
Ubuntu 20.04.1 for genomic data analysis
next-gen
sequencing
genome
updated 4.6 years ago by
tothepoint
▴ 940 • written 4.6 years ago by
Alireza.Tafazoli
• 0
1
vote
0
replies
1.1k
views
Job:
Postdoctoral fellow -- genetic/molecular epidemiology
multiomics
data-analysis
updated 2.3 years ago by
Ram
45k • written 4.6 years ago by
zwangmanu
▴ 10
3
votes
5
replies
4.2k
views
Post-imputation QC GWAS analysis
GWAS
Rstudio
Imputation
TopMed
updated 4.6 years ago by
Biostar
20 • written 5.1 years ago by
AR
• 0
0
votes
1
reply
1.2k
views
Trimming Illumina Seq with TRIMMOMATIC
trimmomatic
GBS
Illumina
4.6 years ago by
giulia.trauzzi
▴ 30
0
votes
2
replies
1.2k
views
bedtools genomecov max function not working correctly
Assembly
bedtools
genomecov
updated 2.3 years ago by
Ram
45k • written 4.6 years ago by
RBright21
▴ 10
4
votes
2
replies
6.4k
views
problems installing HTSeq
RNA-Seq
HTSeq
DEXSeq
updated 4.6 years ago by
Biostar
20 • written 8.4 years ago by
Lila M
★ 1.3k
1
vote
2
replies
1.7k
views
GSEA with GGProfiler2 (?"annotated" vs "known" for background control)
RNA-Seq
GSEA
GGProfiler2
updated 4.6 years ago by
ATpoint
89k • written 4.6 years ago by
drodavis0
• 0
0
votes
0
replies
642
views
database about population data of aquatic animal organisms
databases
4.6 years ago by
eridanus
▴ 40
0
votes
0
replies
653
views
Can I do microarray meta-analysis combinning Induced pluripotent stem cells and neurons?
R
geno
4.6 years ago by
firstorthopedicdoctor
▴ 30
2
votes
2
replies
1.9k
views
Merging PacBio and Nanopore reads
Nanopore
Pacbio
next-gen
long reads
Assembly
updated 4.6 years ago by
harishk0201
▴ 130 • written 4.6 years ago by
Sbrillo
▴ 10
2
votes
7
replies
3.9k
views
Finding assembled transcript sequences from StringTie output
RNA-Seq
StringTie
Assembled Transcripts
Sequences
4.6 years ago by
Jen
▴ 100
2
votes
3
replies
861
views
ENCODE terminology question
sequencing
alignment
updated 4.6 years ago by
i.sudbery
22k • written 4.6 years ago by
ccc
▴ 30
0
votes
5
replies
1.8k
views
MEgene correlated to triat and Gene signficance coorelated to triat
WGCNA
andres.firrincieli
updated 4.4 years ago by
eggerj
▴ 40 • written 4.6 years ago by
adR
▴ 130
121,919 results • Page
712 of 2439
Recent Votes
A: read.table does not read in all rows!
A: read.table does not read in all rows!
A: Binning Over Genes And Calculating The Coverage [Bedops/Bedmap]
Answer: [vg giraffe] Unable to add read group to BAM file
Comment: [vg giraffe] Unable to add read group to BAM file
Answer: [vg giraffe] Unable to add read group to BAM file
Answer: vcf multisample
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Recent Replies
Comment: miRNA low mapping ratings
by
Ant
▴ 50
The first one it's the results from Cutadapter and the second block from miRDeep2.
Comment: miRNA low mapping ratings
by
Ant
▴ 50
Thanks for the reply, when running: cutadapt -a AACTGTAGGCACCATCAAT -M 30 -o example_trimmed.fastq.gz data/xxx.fastq.gz, the sequence le…
Comment: Help with species tree with orthofinder, iqtree and branch labeling
by
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153k
> I don’t have clear species labels in my headers, only sequence IDs. I have not used iqtree, so this is only a thought ... should it be y…
Comment: Help with species tree with orthofinder, iqtree and branch labeling
by
san96
▴ 190
Thank you so much.
Comment: [vg giraffe] Unable to add read group to BAM file
by
saruman
▴ 10
Yes, it seems so. Thank you.
Comment: cellranger mkref fail/error
by
GenoMax
153k
> The thing is that I do not have a genome for these organisms. That is not what `cellranger mkref` is expecting. You could consider alt…
Comment: cellranger mkref fail/error
by
tatsispolychronis
• 0
The thing is that I do not have a genome for these organisms. i made a transcriptome using TRinity and this is what I am feeding it. I do n…
Comment: Genome Assembly QC from BAM files
by
SomeOne
▴ 240
Hi, I am not sure if i can call them good assemblies. Although based on QUAST and BUSCO stats, everything looks too good but somehow i hav…
Comment: cellranger mkref fail/error
by
GenoMax
153k
You need to provide the genome reference for the `--fasta` option as noted in https://www.10xgenomics.com/support/software/cell-ranger/late…
Answer: Methods to analyse structural similarity: co-evolution vs convergence
by
Joe
22k
Without historical data (ancient DNA) there's no way to ever really know this for certain. The best we can do is make inferences based on t…
Answer: vcf multisample
by
Pierre Lindenbaum
166k
eg : https://ega-archive.org/datasets/EGAD50000001683 > Merged VCF file from sporadic Meniere disease cohort (found using https://dat…
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by
GenoMax
153k
Since this saga has been on going for a long time, it will be helpful to add a comment as to how you finally got to this point of what seem…
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by
dthorbur
★ 3.1k
A few comments. 1. Coevolution of a trait between 2 organisms can end up with a convergent structure with another organism. It's not e…
Comment: Genome Assembly QC from BAM files
by
SomeOne
▴ 240
Thank you. Based on the description these two look really what i wanted to see.
Comment: miRNA low mapping ratings
by
i.sudbery
22k
Also, can you just clarify that the output above is from cutadapt or form miRDeep2?
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