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733 results • Page
2 of 15
Sort: Views
Rank
Views
Votes
Replies
19
votes
5
replies
8.9k
views
Tool:
Automatic IGV snapshot script
ChIP-Seq
IGV
updated 13 months ago by
Ram
43k • written 7.2 years ago by
steve
★ 3.5k
83
votes
46
replies
8.9k
views
15 follow
Tool:
ChatGPT optimized for bioinformatics questions
gpt
updated 6 weeks ago by
LauferVA
4.2k • written 10 months ago by
Sasha
▴ 840
6
votes
3
replies
8.8k
views
Tool:
Masc - A Tool For Calculating Mean Fragment Size For Chip-Seq Peak Calling Analysis
chip-seq
updated 10 months ago by
Ram
43k • written 11.2 years ago by
Ian
6.0k
15
votes
19
replies
8.7k
views
6 follow
Tool:
Gemini: Integrative Exploration Of Genetic Variation And Genome Annotations
vcf
database
genome
variation
updated 10 months ago by
Ram
43k • written 11.0 years ago by
Aaronquinlan
12k
16
votes
9
replies
8.7k
views
Tool:
Introducing eLabFTW : free open source electronic lab notebook
eln
open-source
notebook-software
updated 2.4 years ago by
Ram
43k • written 9.7 years ago by
Nico
▴ 190
9
votes
1
reply
8.6k
views
Tool:
Rseqqc And Rna-Seqqc - Quality Control Software For Rna-Seq Data
rna-seq
qc
updated 10 months ago by
Ram
43k • written 11.7 years ago by
Istvan Albert
100k
22
votes
4
replies
8.6k
views
Tool:
Very Bad Things
python
text
updated 16 months ago by
Ram
43k • written 11.2 years ago by
brentp
24k
22
votes
5
replies
8.4k
views
Tool:
Salmon: A fast and versatile new tool for RNA-seq quantification
RNA-Seq
updated 2.1 years ago by
Ram
43k • written 9.4 years ago by
Rob
6.5k
15
votes
11
replies
8.3k
views
Tool:
Arriba: Fast and accurate gene fusion detection from RNA-Seq data
variant-calling
RNA-Seq
cancer
gene-fusion
updated 10 months ago by
Ram
43k • written 6.2 years ago by
uhrigs
▴ 150
48
votes
24
replies
8.2k
views
14 follow
Tool:
Hera: A new tool for RNA-Seq analysis
kallisto
RNA-Seq
STAR
gene-fusion
updated 10 months ago by
Ram
43k • written 6.8 years ago by
sonpham
▴ 580
19
votes
14
replies
8.2k
views
7 follow
Tool:
AfterQC: Automatic Filtering, Trimming, Error Removing and Quality Control for fastq data
PolyG
Quality-Control
Filtering
Fastq
AfterQC
updated 10 months ago by
Ram
43k • written 8.0 years ago by
chen
★ 2.5k
25
votes
19
replies
8.2k
views
10 follow
Tool:
pathfindR - Enrichment Analysis using Active Subnetworks
subnetwork
R
pathway-enrichment
updated 10 months ago by
Ram
43k • written 6.1 years ago by
egeulgen
★ 1.3k
4
votes
0
replies
8.1k
views
Tool:
Snprelate: A Toolset For Relatedness And Principal Component Analysis Of Snp Data
parallel
pca
r
updated 10 months ago by
Ram
43k • written 11.2 years ago by
zx8754
11k
19
votes
5
replies
8.0k
views
Tool:
deepTools: user-friendly tools for the normalization and visualization of deep-sequencing data
Visualisation
RNA-Seq
QC
ChIP-Seq
updated 10 months ago by
Ram
43k • written 9.9 years ago by
Björn
▴ 670
3
votes
1
reply
7.9k
views
Tool:
New ultrafast interval tree implementation for Python: kerneltree
Interval-tree
Python
updated 10 months ago by
Ram
43k • written 6.0 years ago by
endrebak
▴ 960
14
votes
10
replies
7.8k
views
Tool:
ReactomePA: an R/Bioconductor package for reactome pathway analysis and visualization
ReactomePA
R
Visualization
Pathway
Bioconductor
updated 10 months ago by
Ram
43k • written 7.8 years ago by
Guangchuang Yu
★ 2.6k
12
votes
9
replies
7.8k
views
Tool:
gogadget: an R package for go analysis visualization and interpretation
goseq
R
RNA-Seq
gogadget
updated 10 months ago by
Ram
43k • written 7.7 years ago by
Benn
8.3k
19
votes
4
replies
7.7k
views
Tool:
NanoPack: Scripts for long read sequencing data processing and analysis: NanoPlot, NanoFilt, NanoStat, NanoLyse, NanoComp
pacbio
long-reads
oxford-nanopore
updated 10 months ago by
Ram
43k • written 6.6 years ago by
WouterDeCoster
47k
16
votes
16
replies
7.6k
views
6 follow
Tool:
Oncofuse: Prediction Of Driver Gene Fusions From Ngs Data
annotation
fusion
rna-seq
ngs
updated 10 months ago by
Ram
43k • written 10.7 years ago by
mikhail.shugay
3.5k
3
votes
1
reply
7.5k
views
Tool:
Weeder 2.0 - motif discovery tool updated
motif-discovery
chip-seq
weeder
updated 10 months ago by
Ram
43k • written 9.5 years ago by
Ian
6.0k
10
votes
1
reply
7.5k
views
Tool:
Comb-P: Combining Spatially Correlated P-Values
methylation
updated 10 months ago by
Ram
43k • written 11.5 years ago by
brentp
24k
0
votes
2
replies
7.5k
views
Tool:
The script to install the required packages for gene expression analysis using DESeq2 for downstream analysis and visualization
R
RNAseq
installation
DESeq2
8 months ago by
Aditya naman
• 0
10
votes
2
replies
7.4k
views
Tool:
fastp, the ultra-fast FASTQ preprocessing tool, is now on BioConda
fastp
updated 13 months ago by
Ram
43k • written 6.3 years ago by
chen
★ 2.5k
13
votes
2
replies
7.4k
views
Tool:
Software For Detecting Differential Abundance In Meta-Genomic Samples
metagenomics
updated 10 months ago by
Ram
43k • written 11.5 years ago by
Istvan Albert
100k
4
votes
3
replies
7.2k
views
Tool:
Deindexer - A Standalone Demultiplexing Tool For Illumina Platform
illumina
updated 10 months ago by
Ram
43k • written 11.3 years ago by
jingtao09
▴ 110
15
votes
6
replies
7.2k
views
Tool:
Sambamba: High Performance Alternative For Samtools And Picard For Indexing, Sorting And Merging Bam Files
sambamba
bam
samtools
updated 10 months ago by
Ram
43k • written 10.6 years ago by
William
★ 5.3k
20
votes
23
replies
7.2k
views
6 follow
Tool:
EaSeq - Interactive ChIP-seq analysis and visualization (for Windows)
easeq
Windows
Visualization
ChIP-Seq
updated 10 months ago by
Ram
43k • written 8.1 years ago by
Mads Lerdrup
▴ 460
8
votes
10
replies
7.2k
views
7 follow
Tool:
Transcription Factor Binding Sites, Motifs and Expression Profiles from ~10200 ChIP-seq and ~20000 RNA-seq samples
ChIP-Seq
transcription-factor
miRNA
lncRNA
updated 12 months ago by
Ram
43k • written 7.6 years ago by
lsp03yjh
▴ 860
6
votes
3
replies
7.1k
views
Tool:
BioCircos.R: create shiny-friendly interactive multi-track circular plots in R
circos
R
htmlwidgets
shiny
updated 10 months ago by
Ram
43k • written 6.3 years ago by
lvulliard
▴ 60
11
votes
2
replies
7.0k
views
Tool:
fastp (the ultra-fast all-in-one FASTQ preprocessing tool) v0.18.0 released, 2X faster, with many new features.
fastp
QC
updated 10 months ago by
Ram
43k • written 5.8 years ago by
chen
★ 2.5k
5
votes
8
replies
7.0k
views
6 follow
Tool:
Converting MUMmer snps file to a real VCF file
VCF
mummer
SNP
updated 10 months ago by
Ram
43k • written 4.7 years ago by
Matteo Schiavinato
★ 3.6k
9
votes
1
reply
7.0k
views
Tool:
Rsem: Accurate Transcript Quantification From Rna-Seq Data With Or Without A Reference Genome
rna-seq
RSEM
updated 10 months ago by
Ram
43k • written 11.6 years ago by
Istvan Albert
100k
1
vote
4
replies
6.8k
views
Tool:
Jellyfish - Fast, Parallel K-Mer Counting For Dna
jellyfish
updated 10 months ago by
Ram
43k • written 12.0 years ago by
Istvan Albert
100k
5
votes
1
reply
6.6k
views
Tool:
Trim Adapters Of Paired-End Reads (Fastq)
paired-end
adaptor-trimming
ngs
updated 10 months ago by
Ram
43k • written 11.2 years ago by
David Langenberger
11k
3
votes
2
replies
6.6k
views
Tool:
Ancestry: AngularJS module with interactive lineage chart components based on D3.js
visualization
updated 10 months ago by
Ram
43k • written 7.8 years ago by
Lars Schöning
▴ 90
4
votes
2
replies
6.6k
views
Tool:
pdb-tools: a set of Python scripts to manipulate PDB files.
python
pdb
modeling
updated 22 months ago by
Ram
43k • written 9.0 years ago by
João Rodrigues
★ 2.5k
22
votes
8
replies
6.5k
views
Tool:
BioTuring Browser: Making single-cell sequencing data in published studies really accessible!
scRNA-Seq
single-cell
updated 10 months ago by
Ram
43k • written 5.6 years ago by
sonpham
▴ 580
13
votes
1
reply
6.5k
views
Tool:
clusterProfiler: an R package for comparing biological themes among gene clusters
GO
clusterProfiler
KEGG
R
GSEA
updated 10 months ago by
Ram
43k • written 7.8 years ago by
Guangchuang Yu
★ 2.6k
1
vote
0
replies
6.5k
views
Tool:
Free available Supercomputing services - List
Supercomputing
grid
Assembly
annotation
updated 22 months ago by
Ram
43k • written 9.0 years ago by
margxenscienculo
▴ 50
11
votes
14
replies
6.4k
views
6 follow
Tool:
[share] Script to bulk retrieve DNA sequences by protein IDs from GenBank
python
genbank
sequence
cds
protein
updated 2.2 years ago by
Ram
43k • written 9.5 years ago by
qiyunzhu
▴ 130
7
votes
6
replies
6.4k
views
Tool:
PlantTFDB and PlantRegMap: Plant Transcription Factor Database and Plant Regulation Data and Analysis Platform
transcriptional-regulation
enrichment
binding-site
updated 10 months ago by
Ram
43k • written 7.5 years ago by
jin
▴ 80
3
votes
8
replies
6.2k
views
Tool:
MFEprimer-2.0: A Fast Thermodynamics-Based Program For Checking Pcr Primer Specificity
primer
pcr
updated 10 months ago by
Ram
43k • written 11.9 years ago by
Wubin Qu
▴ 170
10
votes
3
replies
6.2k
views
Tool:
GenVisR: Genomic Visualizations in R
visualization
genomic
RNA-Seq
genvisr
updated 10 months ago by
Ram
43k • written 7.9 years ago by
Obi Griffith
20k
11
votes
7
replies
6.2k
views
Tool:
RNA Modification Database and Epitranscriptome Sequencing Data
Epitranscriptome
m5C
m6A
RNA-modification
m1A
updated 20 months ago by
Ram
43k • written 8.5 years ago by
lsp03yjh
▴ 860
13
votes
14
replies
6.1k
views
9 follow
Tool:
open-cravat: variant annotation tool
open-cravat
updated 10 months ago by
Ram
43k • written 5.4 years ago by
slcrick
▴ 260
2
votes
5
replies
6.1k
views
Tool:
umitools - working with UMI incorporated data
UMI
sequencing
updated 10 months ago by
Ram
43k • written 9.8 years ago by
Joe Brown
▴ 70
17
votes
9
replies
6.1k
views
Tool:
Pathomx: Metabolic Pathway Visualisation And Analysis
python
pathway-visualization
updated 10 months ago by
Ram
43k • written 11.1 years ago by
Martin Fitzpatrick
▴ 180
12
votes
5
replies
6.1k
views
Tool:
AGAT - Another Gff/Gtf Analysis Toolkit
gff
gtf
updated 10 months ago by
Ram
43k • written 4.4 years ago by
Juke34
8.5k
19
votes
9
replies
6.1k
views
Tool:
Rlsim, A Package For Simulating Rna-Seq Library Preparation With Parameter Estimation
simulation
rna-seq
pcr
illumina
updated 10 months ago by
Ram
43k • written 11.1 years ago by
Botond Sipos
★ 1.7k
18
votes
2
replies
6.0k
views
Tool:
vcfanno quickly annotate a vcf with other VCFs, BEDs, BAMs
VCF
variant-annotation
updated 10 months ago by
Ram
43k • written 8.8 years ago by
brentp
24k
733 results • Page
2 of 15
Recent Votes
Answer: NGS forensics: how to know if data is fabricated
Comment: NGS forensics: how to know if data is fabricated
Comment: NGS forensics: how to know if data is fabricated
NGS forensics: how to know if data is fabricated
Comment: NGS forensics: how to know if data is fabricated
Answer: NGS forensics: how to know if data is fabricated
Answer: NGS forensics: how to know if data is fabricated
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Recent Replies
Comment: NGS forensics: how to know if data is fabricated
by
i.sudbery
19k
I don't follow your argument for distinguishing between genomic contamination and freud. A data set being bad in terms of genomic contamin…
Comment: What does it mean single base resolution in sequencing?
by
jinyu
▴ 10
Thank you for your detail and great explanation. I do need more time to understand these. And there is still something compuzzling me. For …
Answer: Is it possible to bulk download files from GEO repository?
by
atharvakarkare14
▴ 10
Try using this library [GEOparse][1] [1]: https://github.com/guma44/GEOparse
Answer: How many reads for WGS Sequencing?
by
Ruqaiya
• 0
OK. Problem solved. The problem was from my end. Thank you both for helping !!
Comment: NGS forensics: how to know if data is fabricated
by
Mensur Dlakic
★ 27k
Appreciate the suggestion, but that ship has sailed and reached the other shore. This happened 10+ years ago. To the best of my knowledge n…
Comment: Figures are disappeared from html report of SnpEff
by
analyst
▴ 30
Files are not opening in any of the computer (ubuntu/windows). I rereun snpEff annotation but still output html files are having missing im…
Comment: Figures are disappeared from html report of SnpEff
by
analyst
▴ 30
I reinstalled nodejs: > sudo apt-get install nodejs Its already up to date with version v10.19.0
Answer: NGS forensics: how to know if data is fabricated
by
Prash
▴ 280
Mensur, if I were you, I'd probably contact the CA directly and check with him whether they have reproduced the works recently. There coul…
Comment: NGS forensics: how to know if data is fabricated
by
noodle
▴ 560
Working on it - it's actually a bit difficult. Low coverage of ribosomal proteins. Low coverage of housekeeping genes ...I'm trying to find…
Comment: NGS forensics: how to know if data is fabricated
by
noodle
▴ 560
I'm a bit against pubpeer - have you ever posted there? My gripe with them is that the posts are heavily moderated and EDITED to the point…
Comment: NGS forensics: how to know if data is fabricated
by
Philipp Bayer
8.4k
Thanks Mensur! I'd add that in 9 out of 10 cases, you won't receive a reply to a request for raw data. That's just how scientists are, does…
Comment: How many reads for WGS Sequencing?
by
Ruqaiya
• 0
I had downloaded the two files in a similar manner actually.
Comment: How many reads for WGS Sequencing?
by
Ruqaiya
• 0
ok, i'll try to use fastp. I have only used trimmomatic and cutadapt till now and they dont identify on its own. Except the graph in fastqc…
Comment: How many reads for WGS Sequencing?
by
Ruqaiya
• 0
got it! even if i'm doing the assembly for paired end with both the files do i have set the threshold to 1000bp ?
Comment: NGS forensics: how to know if data is fabricated
by
Philipp Bayer
8.4k
i've been in our org trying to push such a detector, our use-case is much more limited: I want to make simulated eDNA libraries as real as …
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