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122,037 results • Page
2 of 2441
Sort: Rank
Rank
Views
Votes
Replies
1
vote
4
replies
559
views
Problems with PacBio's Improved Phased Assembler (IPA)
pacbio
hifi
assembly
genome
7 days ago by
Panos
★ 1.8k
0
votes
6
replies
615
views
downloading raw bam files from pacbio sequencer
raw
bam_file
raw_subreads
reads
updated 8 days ago by
GenoMax
154k • written 9 days ago by
pranavdatar01
• 0
0
votes
0
replies
286
views
Best way to map biological pathways to cancer hallmarks using PLMs (without building models)?
PLM
mapping
LLM
extraction
Relation
8 days ago by
DEPANSHI
• 0
1
vote
2
replies
624
views
installation of package ‘DESeq2’ had non-zero exit status
Bioinformatics
updated 8 days ago by
GenoMax
154k • written 8 days ago by
Sarita
• 0
0
votes
1
reply
335
views
Checkm results differ from database info
Checkm
updated 4 days ago by
Ram
45k • written 8 days ago by
alevbozan18
• 0
0
votes
2
replies
1.2k
views
Transverse data
EXCEL
Unix
updated 8 days ago by
basu
• 0 • written 2.7 years ago by
Sidra
• 0
0
votes
0
replies
278
views
Is this the correct order of steps in GATK germline cohort variant calling (VQSR workflow)?
gVCF
VCF
GATK
VQSR
8 days ago by
Ramnaresh
• 0
0
votes
0
replies
296
views
How to select background metabolite sets for differential metabolite enrichment analysis?
enrichment
ORA
8 days ago by
Edward
• 0
1
vote
3
replies
475
views
Pseudogene - scarce info
pseudogene
mastersdegree
updated 5 days ago by
ATpoint
89k • written 9 days ago by
mf810
▴ 10
1
vote
4
replies
1.9k
views
HIV NL4-3 transcriptome fasta
rna-seq
CLIP-seq
updated 9 days ago by
Ales
▴ 90 • written 5.5 years ago by
xiaoleiusc
▴ 140
1
vote
1
reply
369
views
Doubt on docking
docking
active
site
bioinformatics
updated 9 days ago by
Mensur Dlakic
★ 30k • written 9 days ago by
Ria
• 0
1
vote
0
replies
279
views
News:
Online course: RNA sequencing data analysis using R and Bioconductor - 3–14 November
R
DifferentialExpressionAnalysis
RNAseq
Bioconductor
9 days ago by
Physalia-courses
★ 2.7k
6
votes
3
replies
483
views
Nextflow MultiQC runs multiple times due to FASTQC zip name collisions
fastqc
nextflow
multiqc
updated 9 days ago by
Phil Ewels
★ 1.5k • written 10 days ago by
DdogBoss
▴ 30
0
votes
1
reply
5.1k
views
News:
::Last Call:: In-Person Workshop - NGS Epigenomics Data Analysis (November 3-5 in Munich) - BS-Seq, ChIP-Seq, ATAC-Seq, ...
chip-seq
atac-seq
bs-seq
9 days ago by
ecSeq Bioinformatics
▴ 20
0
votes
2
replies
5.7k
views
Best set of tools / workflows for predicting the biosynthesis pathways of complex organic molecules
ngs
pathways
bioinformatics
updated 10 days ago by
ehaag
▴ 100 • written 25 days ago by
Mark
▴ 60
12
votes
15
replies
3.6k
views
6 follow
Tools to simulate Illumina short read sequences and ONT long reads with a reference genome
simulate
reads
bioinformatics
short
short-read
1 day ago by
PolenP
▴ 10
1
vote
1
reply
353
views
Corresponding BAM files
BAM
SRA
GEO
FASTQ
updated 10 days ago by
GenoMax
154k • written 10 days ago by
aj123
▴ 130
0
votes
2
replies
1.8k
views
Analyzing CRISPR and RNAi genome wide screens
CRISPR
RNAi
meta analysis
updated 10 days ago by
Meisam
▴ 250 • written 7.3 years ago by
spacemorrissey
▴ 280
0
votes
3
replies
2.8k
views
meta data analysis for clustering
meta-analysis
clustering
functional genomics
updated 10 days ago by
Meisam
▴ 250 • written 7.7 years ago by
jiwpark00
▴ 230
2
votes
9
replies
3.5k
views
GTF file for HIV strain pNL4-3
HIV
annotation
mapping
updated 10 days ago by
Ales
▴ 90 • written 7.3 years ago by
caggtaagtat
★ 1.9k
0
votes
1
reply
313
views
Diffbind or DESEQ2 Chipseq data
Chipseq
DESEQ2
Diffbind
5 days ago by
Irene
• 0
0
votes
0
replies
270
views
Job:
Postdoctoral Fellowship at the American Museum of Natural History's Richard Gilder Graduate School
Postdoctoral
Fellowship
10 days ago by
Info-rggs
▴ 20
0
votes
0
replies
265
views
News:
Autumn School in Bioinformatics - online, 20–24 October
NGS
Phylogenomics
RNAseq
Singularity
Docker
10 days ago by
Physalia-courses
★ 2.7k
1
vote
4
replies
605
views
Dorado in PowerShell on Windows
Windows
on
PowerShell
in
Dorado
updated 9 days ago by
jared.andrews07
★ 19k • written 10 days ago by
sbissi102
▴ 10
1
vote
0
replies
284
views
Is this an appropriate command for estimating contaminatin in a germline WGS sample using GATK?
gatk
10 days ago by
curious
▴ 900
1
vote
4
replies
563
views
Which aligner is more suitable for ONT R10.4.1 Dorado-corrected reads: minimap2 or winnowmap?
winnowmap
minimap2
R10.4.1
Nanopore
10 days ago by
tungsega
▴ 10
2
votes
2
replies
440
views
Nextflow: How to format input tuple for STAR_ALIGN process with STAR index directory
nextflow
11 days ago by
DdogBoss
▴ 30
4
votes
4
replies
543
views
how to respond that my research does not have experimental validation
rebuttal
updated 11 days ago by
Mensur Dlakic
★ 30k • written 11 days ago by
nuorain
▴ 40
6
votes
7
replies
756
views
Quantification using salmon in alignment-based mode after minimap2 run
nanopore
ont
salmon
3 days ago by
Assa Yeroslaviz
★ 1.9k
1
vote
1
reply
368
views
infercnv error at STEP 18 - file descriptor is too large for select()
R
10x
singlecell
infercnv
11 days ago by
yura.grabovska
▴ 850
0
votes
0
replies
253
views
News:
online course - Environmental Metagenomics
Illumina
Metagenomics
Nanopore
MAGs
11 days ago by
Physalia-courses
★ 2.7k
0
votes
1
reply
308
views
Need Help : JGI IMG Bulk Download
Bioinformatics
updated 11 days ago by
GenoMax
154k • written 11 days ago by
Ananaya
• 0
0
votes
4
replies
456
views
How to convert gff to Sequin format with gff3-to-tbl?
genome
annotation
conversion
Sequin
gff
updated 12 days ago by
GenoMax
154k • written 12 days ago by
marongiu.luigi
▴ 770
0
votes
1
reply
445
views
How much coverage is needed for high-quality phylogenetic and admixture analyses using short-read WGS in plants?
coverage
updated 10 days ago by
colindaven
8.0k • written 12 days ago by
rosaceae
• 0
1
vote
10
replies
3.1k
views
Collect COV file by BedCoverage
copynumbervariation
ClinCNV
ngs
updated 4.3 years ago by
German.M.Demidov
★ 3.0k • written 4.3 years ago by
Ishak
▴ 20
0
votes
1
reply
326
views
gnomad par region variants
region
variant
par
gnomad
updated 13 days ago by
benformatics
4.2k • written 14 days ago by
a615ebfb
▴ 60
0
votes
2
replies
402
views
Forum:
Help with Ideathon
PGS
PRS
brainstorming
genomics
bioinformatics
13 days ago by
V K
• 0
2
votes
2
replies
437
views
Gene expression equivalent of polygenic risk score ?
expression
gene
14 days ago by
Picasa
▴ 690
0
votes
1
reply
501
views
Help interpreting BLASTn results and phylogenetic tree for genetics practical
student
updated 15 days ago by
GenoMax
154k • written 16 days ago by
simonlydialm
• 0
0
votes
0
replies
281
views
News:
Introduction to CRISPR for Ecology and Evolution Studies (13–16 Oct, online)
GenomeEditing
Cas9
CRISPR
Evolution
15 days ago by
Physalia-courses
★ 2.7k
0
votes
2
replies
473
views
tximport error (medianLengthOverIsoform)
DTU
RNA-seq
tximport
10 days ago by
LGG
• 0
0
votes
8
replies
862
views
Errors with RSEM/bowtie2
RNA-seq
bowtie2
RSEM
Trinity
11 days ago by
Olivia
• 0
3
votes
1
reply
672
views
With 10x Visum HD : How to map the barcode id to the barcode sequence ?
10x
barcode
Visium
16 days ago by
sacha
★ 2.5k
0
votes
0
replies
327
views
Job:
Genetics for Biodiversity Conservation Korea - Ecuador
Ecuador
biodiversity
Korea
updated 15 days ago by
colindaven
8.0k • written 16 days ago by
Pablo
• 0
0
votes
1
reply
433
views
help with modkit on nanopore sequencing data.
mokit
nanopore
help
updated 15 days ago by
andres.firrincieli
3.9k • written 16 days ago by
felix.adams
• 0
1
vote
0
replies
348
views
News:
FastTrack Bioinformatics - Online Course in Bioinformatics
handbook
biostar
16 days ago by
Istvan Albert
103k
3
votes
1
reply
857
views
Dictys refuses to use CUDA supported pytorch during installation
python
conda
gpu
17 days ago by
zwjiang
▴ 30
0
votes
0
replies
594
views
Haploview LD plot unespected results
Haploview
SNPs
17 days ago by
chiuni2308
• 0
0
votes
0
replies
664
views
News:
online course: Efficient Data Analysis with data.table in R - 8 October
R
Programming
DataTable
17 days ago by
Physalia-courses
★ 2.7k
1
vote
0
replies
674
views
Tool:
Modernized RNA-MuTect pipeline for tumor-only RNA-seq somatic variant calling
somatic
rna-seq
17 days ago by
darklings
▴ 590
122,037 results • Page
2 of 2441
Recent Votes
Answer: High Variability when Peak Calling with SEACR
A: Get chromosome sizes from fasta file
How to keep the top hits only in the output file of hmmscan?
A: How to keep the top hits only in the output file of hmmscan?
ProbeID to Gene Symbol Mapping in Microarray data analysis using R
Answer: Unique insertion sites Calculation from Himar1 C9 based TnSeq
Answer: Choosing enrichment analysis tool
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Answer: DE analysis in nascent RNA Seq based on intron sequences
by
dsull
★ 7.7k
Yes, that’s fine; I don’t see why nascent transcripts should be treated differently than mature transcripts in DE analysis.
Comment: High Variability when Peak Calling with SEACR
by
RD
▴ 30
Hi Jared, I’m trying to figure out the right parameters to use with MACS3 for CUT&RUN data. My understanding is that it’s best to convert t…
Answer: SNP calling ONT sequenced files
by
Момчил
▴ 10
Yes, one can say that ONT reads do still have higher error rates in comparison to Illumina short reads, but the situation has improved sign…
Comment: MOuse Testis Enhancer region
by
GenoMax
154k
That web site is off-line for everyone. You will have to look for an alternate option.
Answer: Is there a way to produce/convert nhmmer output to a bed file?
by
colindaven
8.0k
To make it a bit clearer for nhmmer specifically, I used the following. This is code used in nextflow. # run nhmmer nhmm…
Comment: reference-guided assembly tools for short read data?
by
lieven.sterck
16k
there are several options to choose from, doing a quick google search will give you a lot. The main thing to keep in mind is to choose one …
Comment: Python deconvolution tools for bulk RNA-seq data
by
Arup Ghosh
3.4k
Check the [Bulk2Single][1] option from [OmicVerse][2] framework. [1]: https://omicverse.readthedocs.io/en/latest/Tutorials-bulk2single/…
Comment: reference-guided assembly tools for short read data?
by
michael.ante
★ 4.0k
I don't know how well it works for plants, but I worked with [Saute][1] and it was doing well for reference based assemblies. [1]: http…
Comment: hisat2 error-Paired end reads not equal or lack of RAM/disk space?
by
ATpoint
89k
Most likely a download artifact. First I would re-download and inly if that fails again then do repairing. ftp is primitive, it's just hit …
Answer: Python deconvolution tools for bulk RNA-seq data
by
ATpoint
89k
Imo you are approaching this the wrong way. R packages for deconvolution that are heqavily used and cited do exist, for example MuSiC and B…
Comment: MOuse Testis Enhancer region
by
Bioinformatics_16
• 0
@genomax Do you have access to this list? If so, could you please share it? I need it urgently.
Comment: HDOCK Server Error!
by
Jannatul Ferdous
• 0
Tried that but unfortunately, the problem still persists :( Thanks for your response though!
Answer: Unique insertion sites Calculation from Himar1 C9 based TnSeq
by
LChart
5.1k
While Himar1 inserts in TA motifs, the library is generated following restriction enzyme treatment (Mmrl) and ligation. The Mmrl sequence i…
Comment: Is it possible to do standard GSEA in R?
by
mbramble
• 0
See discussion at https://support.bioconductor.org/p/9142651/#9142680 concerning issues with preranked gsea.
Comment: BWA-MEM with an array of files
by
LChart
5.1k
For solution 1, because bwa streams the data, you can save some space by using a named pipe: ```bash mkfifo Sample_23/concat.R1.fq.gz find…
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