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517 results • Page
2 of 11
Sort: replies
Rank
Views
Votes
Replies
9
votes
12
replies
4.6k
views
Tool:
fastp v0.9 released: an all-in-one FASTQ preprocessor (QC, adapters, trimming, quality filtering / cutting, splitting output ... )
fastq
fastp
open-source
updated 10 months ago by
Ram
43k • written 6.5 years ago by
chen
★ 2.5k
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 11 months ago by
Ram
43k • written 6.3 years ago by
uhrigs
▴ 150
7
votes
11
replies
3.2k
views
Tool:
Graphical User Interface for creating an automated RNA-Sequencing Pipeline via Kallisto and DESeq2
DESeq2
kallisto
RNA-Seq
updated 10 months ago by
Ram
43k • written 5.4 years ago by
Anthony.Knox
▴ 60
21
votes
11
replies
11k
views
Tool:
Segemehl: A Fast One-Stop-Shop Mapping Tool
mapping
next-gen
updated 10 months ago by
Ram
43k • written 11.6 years ago by
David Langenberger
11k
17
votes
11
replies
11k
views
6 follow
Tool:
Pyfaidx: Efficient, "Pythonic" Random Access To Fasta Files Using Samtools-Compatible Indexing
fasta
python
samtools
updated 10 months ago by
Ram
43k • written 10.2 years ago by
Matt Shirley
10k
7
votes
10
replies
1.5k
views
Tool:
SamReadViewer - A small utility to visualise read alignment directly from sam format without reference.
samreadviewer
updated 11 months ago by
Ram
43k • written 3.6 years ago by
Juke34
8.6k
23
votes
10
replies
12k
views
Tool:
ggtree: phylogenetic tree visualization and annotation
ggtree
phylogeny
visualization
updated 10 months ago by
Ram
43k • written 7.9 years ago by
Guangchuang Yu
★ 2.6k
11
votes
10
replies
2.3k
views
Tool:
[Crushing the bureaucracy in bioinformatics] Introducing Skymap-JupyterHub: accessing and utilizing reprocessed expression/ allelic read count profil…
SNP
RNA-Seq
ChIP-Seq
updated 10 months ago by
Ram
43k • written 5.8 years ago by
btsui
▴ 300
3
votes
10
replies
1.7k
views
Tool:
Quick & dirty DNA coordinates in any mac app
sequence
alignment
updated 10 months ago by
Ram
43k • written 6.2 years ago by
rleach
▴ 180
14
votes
10
replies
7.9k
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 7.9 years ago by
Guangchuang Yu
★ 2.6k
34
votes
9
replies
11k
views
7 follow
Tool:
Bwa-Meth: Align And Tabulate Bs-Seq Reads
methylation
updated 10 months ago by
Ram
43k • written 10.2 years ago by
brentp
24k
7
votes
9
replies
4.0k
views
Tool:
VCF-simplify: a VCF simplification tool.
VCF
variants
genome
updated 11 months ago by
Ram
43k • written 6.1 years ago by
kirannbishwa01
★ 1.6k
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 7.8 years ago by
Benn
8.3k
4
votes
9
replies
2.7k
views
Tool:
CANEapp, a user-friendly application for automated next generation transcriptomic data analysis
RNA-Seq
written 8.3 years ago by
dvelmeshev
• 0
17
votes
9
replies
17k
views
6 follow
Tool:
ggrepel: repel overlapping text labels in ggplot2
R
visualization
updated 11 months ago by
Ram
43k • written 8.4 years ago by
Kamil
★ 2.3k
9
votes
9
replies
4.7k
views
Tool:
pyCirclize - Circular visualization in Python
visualization
circos
matplotlib
genome
python
updated 9 months ago by
shuo
• 0 • written 17 months ago by
moshi
▴ 150
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 11 months ago by
Ram
43k • written 11.1 years ago by
Botond Sipos
★ 1.7k
3
votes
9
replies
3.6k
views
Tool:
Download all refseq/genbank bacterial genomes from NCBI
genome
sequencing
updated 10 months ago by
Ram
43k • written 7.3 years ago by
johnsrc06
▴ 10
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
8
votes
9
replies
8.9k
views
Tool:
Lofreq: A Fast And Sensitive Variant-Caller For Inferring Single-Nucleotide Variants From Ngs Data
snp
next-gen
somatic-variant
updated 10 months ago by
Ram
43k • written 11.6 years ago by
Andreas
★ 2.5k
15
votes
9
replies
3.4k
views
Tool:
FlexiDot: highly customizable, ambiguity-aware dotplots
dotplot
visualization
sequence-analysis
updated 10 months ago by
Ram
43k • written 6.0 years ago by
toheitka
▴ 230
5
votes
8
replies
7.1k
views
6 follow
Tool:
Converting MUMmer snps file to a real VCF file
VCF
mummer
SNP
updated 11 months ago by
Ram
43k • written 4.7 years ago by
Matteo Schiavinato
★ 3.6k
2
votes
8
replies
3.7k
views
Tool:
Mirnakey - A Software Pipeline For The Analysis Of Microrna Deep Sequencing Data
mirna
updated 10 months ago by
Ram
43k • written 11.7 years ago by
Istvan Albert
100k
6
votes
8
replies
4.9k
views
Tool:
Read-based phasing with WhatsHap
phasing
updated 10 months ago by
Ram
43k • written 7.4 years ago by
Marcel M
▴ 100
10
votes
8
replies
1.9k
views
6 follow
Tool:
"bioalcidae, samjs and vcffilterjs" published in bioinformatics.
jvarkit
bam
vcf
javascript
java
updated 10 months ago by
Ram
43k • written 6.5 years ago by
Pierre Lindenbaum
161k
3
votes
8
replies
736
views
Tool:
Generate unit-tested, ready-to-run pipelines using natural language prompting
NGS
pipeline
genomics
cloud
AI
updated 3 months ago by
Ram
43k • written 3 months ago by
Kevin
▴ 50
3
votes
8
replies
6.3k
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 12.0 years ago by
Wubin Qu
▴ 170
22
votes
8
replies
6.6k
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
8
replies
4.3k
views
Tool:
MSigDB for Multiple Organisms in a Tidy Data Format
msigdb
pathways
R
gsea
updated 11 months ago by
Ram
43k • written 6.1 years ago by
igor
13k
13
votes
7
replies
9.8k
views
Tool:
Command-Line Software For Bigwig Data
bigwig
updated 10 months ago by
Ram
43k • written 10.5 years ago by
andypohl
▴ 90
54
votes
7
replies
4.0k
views
6 follow
Tool:
Looking For People That Would Try A Custom Genome Viewer That I Wrote For Bioinformatics
genome-viewer
updated 10 months ago by
Ram
43k • written 11.0 years ago by
chbelhumeur2000
▴ 40
9
votes
7
replies
3.0k
views
Tool:
DiffBind 3.0: Extensive updates in Bioconductor 3.12
DiffBind
ChIP-Seq
diffbind
ATAC-seq
chipseq
updated 11 months ago by
Ram
43k • written 3.5 years ago by
Rory Stark
★ 2.0k
12
votes
7
replies
3.2k
views
Tool:
Chromozoom: The Genome Browser That Lets You Fly!
genome-browser
browser
updated 10 months ago by
Ram
43k • written 11.2 years ago by
Istvan Albert
100k
6
votes
7
replies
2.5k
views
Tool:
Workflow for structural variants from long read sequencing data
structural-variation
pacbio
nanopore
snakemake
updated 10 months ago by
Ram
43k • written 5.6 years ago by
WouterDeCoster
47k
4
votes
7
replies
1.4k
views
Tool:
Elloreas, a new genome assembler
Assembly
next-gen
updated 11 months ago by
Ram
43k • written 3.9 years ago by
shelkmike
★ 1.2k
7
votes
7
replies
4.7k
views
Tool:
Variant Annotation, Analysis and Search Tool - VAAST2
VAAST2
VAAST
updated 10 months ago by
Ram
43k • written 10.0 years ago by
Zev.Kronenberg
12k
28
votes
7
replies
11k
views
Tool:
Quast Is A Convenient Tool For Assembly Evaluation
assembly
quality
updated 10 months ago by
Ram
43k • written 11.2 years ago by
Nikolay Vyahhi
★ 1.3k
6
votes
7
replies
3.1k
views
Tool:
MutScan: detect and visualize target mutations by just scanning FastQ, 50X faster than normal pipelines
Mutation
FastQ
MutScan
OpenGene
updated 10 months ago by
Ram
43k • written 7.1 years ago by
chen
★ 2.5k
2
votes
7
replies
2.9k
views
Tool:
An online cute tool to query tumor-gene data from MSK-IMPACT project
MSK-IMPACT
tumor
mutation
MSK
updated 10 months ago by
Ram
43k • written 7.0 years ago by
chen
★ 2.5k
2
votes
7
replies
2.7k
views
Tool:
metaflagstat.py - painless bam/sam read flag counting
samtools
bam
updated 10 months ago by
Ram
43k • written 9.7 years ago by
John
13k
5
votes
7
replies
3.7k
views
Tool:
CircTools: Softwares for Discovering circRNA-microRNA Interactions from CLIP-Seq Datasets
circRNA
CLIP-seq
microRNA
RNA-seq
Interactome
updated 10 months ago by
Ram
43k • written 6.0 years ago by
lsp03yjh
▴ 860
4
votes
7
replies
4.6k
views
6 follow
Tool:
MAGERI: a software tool for calling rare variants and detecting circulating tumor DNA from UMI-tagged high-throughput sequencing data
rare-variant
resequencing
umi
ctDNA
updated 3 months ago by
blid11
• 0 • written 7.0 years ago by
mikhail.shugay
3.5k
9
votes
7
replies
3.6k
views
Tool:
metaViC: Virus metagenomics pipeline for unknown host or in absence of a host genome
Assembly
metagenomics
ngs
updated 10 months ago by
Ram
43k • written 7.7 years ago by
Sej Modha
5.3k
3
votes
7
replies
1.4k
views
Tool:
New method for protein secondary structure prediction
protein
secondary-structure
updated 11 months ago by
Ram
43k • written 4.7 years ago by
vytarasov
▴ 180
13
votes
6
replies
5.2k
views
Tool:
csvtk - a cross-platform, efficient, practical and pretty CSV/TSV toolkit
CSV
Golang
TSV
9 months ago by
shenwei356
8.5k
13
votes
6
replies
4.9k
views
Tool:
GAWN - Genome Annotation Without Nightmares
genome-annotation
updated 10 months ago by
Ram
43k • written 6.8 years ago by
Eric Normandeau
11k
0
votes
6
replies
1.5k
views
Tool:
Script: Downloading fastq files from ENA database
next-gen-sequencing
RNA-Seq
updated 11 months ago by
Ram
43k • written 3.3 years ago by
jayeshkumarsundaram
• 0
8
votes
6
replies
5.9k
views
Tool:
chromoMap- R package for Interactive visualization and Annotation of chromosomes or regions of any living organism.
annotation
R
genome
visualization
updated 11 months ago by
Ram
43k • written 5.1 years ago by
lakshayanand15
▴ 80
12
votes
6
replies
3.5k
views
Tool:
Variant annotation and filtration server ALAPY Genome Explorer (AGx)
vcf
variant-annotation
variant-interpretation
updated 10 months ago by
Ram
43k • written 7.0 years ago by
Petr Ponomarenko
★ 2.8k
6
votes
6
replies
4.8k
views
Tool:
Reading/ Writing FASTA files in Java
FASTA
Java
updated 10 months ago by
Ram
43k • written 9.4 years ago by
alex
• 0
517 results • Page
2 of 11
Recent Votes
Comment: Faster Needleman-Wunsch rapid global alignment of two sequences?
Answer: Details on salmon index
Comment: zero TPM for many gene including housekeeping when using kallisto
Sequence Alignment from Scratch with BWA
Answer: mitochondrial genome assembly pipeline
Comment: Help! Reconstruction of locus, order contigs
Comment: In one PCA plot, can I calculate the percentage of different factors that contri
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Recent Replies
Comment: Help! Reconstruction of locus, order contigs
by
dthorbur
★ 2.0k
I don't understand your comment. What do you mean? > my idea is not to have to write it down If you have an alignment already, why can't…
Comment: Help! Reconstruction of locus, order contigs
by
GenoMax
142k
Please use `ADD REPLY/ADD COMMENT` when responding to existing content. `SUBMIT ANSWER` is for new answers to the original question.
Comment: Details on salmon index
by
Rob
6.6k
Hi Lorenzo, That is correct. The initial version of salmon used the RapMap index explained above. When we published the selective align…
Comment: Help! Reconstruction of locus, order contigs
by
BATMAN
• 0
Thanks for your reply, my idea is not to have to write it down. What I have is an alignment of the .gbk from the progressiveMauve. It would…
Comment: Faster Needleman-Wunsch rapid global alignment of two sequences?
by
Gabriel R.
★ 2.9k
I did some digging aroumd, no static binary. Plus it seems you need to roll your own program.
Comment: Faster Needleman-Wunsch rapid global alignment of two sequences?
by
Gabriel R.
★ 2.9k
We tested it, however, it does not seem to produce a fast a file of the results or anything that we can easily parse. It produces a CIGAR a…
Comment: zero TPM for many gene including housekeeping when using kallisto
by
ashkan
▴ 160
@atpoint yes but for example for the kallisto results I have expression for 2080 genes (transcripts) and the rest are 0 but in my STAR resu…
Comment: In one PCA plot, can I calculate the percentage of different factors that contri
by
marco.barr
▴ 130
great team work! why can't you access and do the calculation for the other components too? can't you extract the information from the other…
Comment: zero TPM for many gene including housekeeping when using kallisto
by
ATpoint
82k
Yes, but this is what I am saying: GAPDH in human has at least 6 annotated transcripts. Have you looked at all of them? Maybe that particul…
Comment: zero TPM for many gene including housekeeping when using kallisto
by
ashkan
▴ 160
@atpoint these are from PBMC. no they are different genes. for example ENST00000229239.10 is GAPDH. in STAR I got a lot of reads aligned …
Comment: zero TPM for many gene including housekeeping when using kallisto
by
ashkan
▴ 160
@dariober: I have to use kallisto for our downstream pipeline.
Comment: zero TPM for many gene including housekeeping when using kallisto
by
ATpoint
82k
Which celltype is this? Are these transcripts of the same gene, and of which gene?
Comment: zero TPM for many gene including housekeeping when using kallisto
by
ashkan
▴ 160
@atpoint the question is updated. the first command shows how the index is built.
Comment: Help! Reconstruction of locus, order contigs
by
dthorbur
★ 2.0k
Is the *de novo* annotation required for each contig? Reconstructing homologous regions in many genomes can be tricky regardless, but is es…
Comment: In one PCA plot, can I calculate the percentage of different factors that contri
by
diqixiaoyaoer
▴ 20
You can have a look on my answer. I have post it below.
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