Learn more: github.com/telatin/seqfu2 [2/2]
Learn more: github.com/telatin/seqfu2 [2/2]
⏰Oct 16th
➡️Research fellowship
✅Msc Students, at the time of the start of the contract
✅Knowledge of computational methods, namely FASTQ data processing & QC
✅Analysis of predictive models
👉https://tinyurl.com/279tsmj3
#i3Sjobs
⏰Oct 16th
➡️Research fellowship
✅Msc Students, at the time of the start of the contract
✅Knowledge of computational methods, namely FASTQ data processing & QC
✅Analysis of predictive models
👉https://tinyurl.com/279tsmj3
#i3Sjobs
We present SCAR, the perfect tool for assessing the impact of #ancientDNA damage on analyses
Validation tests show how damage massively impacts heterozygosity estimates 😨
Check it out here
www.biorxiv.org/content/10.6...
We present SCAR, the perfect tool for assessing the impact of #ancientDNA damage on analyses
Validation tests show how damage massively impacts heterozygosity estimates 😨
Check it out here
www.biorxiv.org/content/10.6...
PhD required, start date hopefully Nov 1! (end date Sep 30 2028)
Please share!
abetterscientist.wordpress.com/2026/09/29/p...
PhD required, start date hopefully Nov 1! (end date Sep 30 2028)
Please share!
abetterscientist.wordpress.com/2026/09/29/p...
YEARS OF FILE EXTENSIONS yet NO REAL WORLD USE FIND for anything except .txt
".py" ".cpp" ".fastq" - statements dreamed up by the utterly deranged.
"Hello I'd like to open pdf please"
THEY HAVE PLAYED US FOR ABSOLUTE FOOLS
YEARS OF FILE EXTENSIONS yet NO REAL WORLD USE FIND for anything except .txt
".py" ".cpp" ".fastq" - statements dreamed up by the utterly deranged.
"Hello I'd like to open pdf please"
THEY HAVE PLAYED US FOR ABSOLUTE FOOLS
Still measures the fastest of the bunch, though AdapterRemoval v3 isn't too far behind.
Now with support for streaming interleaved FASTQ!
🧬 🖥️
github.com/fulcrumgenom...
Still measures the fastest of the bunch, though AdapterRemoval v3 isn't too far behind.
Now with support for streaming interleaved FASTQ!
🧬 🖥️
github.com/fulcrumgenom...
`seqfu less` can do that! You can scroll, search for motives and see intuitive colored bars representing quality values.
Check it out here: telatin.github.io/seqfu2/tools...
`seqfu less` can do that! You can scroll, search for motives and see intuitive colored bars representing quality values.
Check it out here: telatin.github.io/seqfu2/tools...
Meet Cleaver-X — one binary for:
✂️ Trimming + QC
🧬 FASTA/FASTQ/SAM/BAM
📊 Counting + demux
⚡ Constant-memory streaming
180 MB in 0.17 sec. ~7 MB RAM.
No Python. No C/C++.
Just Rust. 🦀
#Rust #rustsky
Crates
crates.io/crates/Cleav...
Meet Cleaver-X — one binary for:
✂️ Trimming + QC
🧬 FASTA/FASTQ/SAM/BAM
📊 Counting + demux
⚡ Constant-memory streaming
180 MB in 0.17 sec. ~7 MB RAM.
No Python. No C/C++.
Just Rust. 🦀
#Rust #rustsky
Crates
crates.io/crates/Cleav...
We tried to make it nicer, but also introduced new in-browser applets.
Try these two:
- 📊 STATS to calculate N50 and plots, for one or more files, or
- 🔍 LESS to have a small preview of FASTQ files with quality, oligo match and more.
telatin.github.io/seqfu2/
We tried to make it nicer, but also introduced new in-browser applets.
Try these two:
- 📊 STATS to calculate N50 and plots, for one or more files, or
- 🔍 LESS to have a small preview of FASTQ files with quality, oligo match and more.
telatin.github.io/seqfu2/
I have, so I made a tool for it.
PlainMap handles mixed SE/PE, different FASTQ formats, modern + #aDNA, pilot testing, and restartable runs then gives you a BAM + stats.
arxiv.org/abs/2609.183...
I have, so I made a tool for it.
PlainMap handles mixed SE/PE, different FASTQ formats, modern + #aDNA, pilot testing, and restartable runs then gives you a BAM + stats.
arxiv.org/abs/2609.183...
Small enough to keep an entire cohort online instead of banishing reads to cold storage. But to be useful, the representation should be accurate/faithful.
Small enough to keep an entire cohort online instead of banishing reads to cold storage. But to be useful, the representation should be accurate/faithful.
expressrna.org
#iCLIP #bioinformatics #clip #expressRNA
expressrna.org
#iCLIP #bioinformatics #clip #expressRNA
👉 github.com/Nephrogenomi...
#Nephrology #Genomics #RareDisease #ADTKD #MUC1 #Bioinformatics #OpenSource
👉 github.com/Nephrogenomi...
#Nephrology #Genomics #RareDisease #ADTKD #MUC1 #Bioinformatics #OpenSource
Please see the changelog: https://github.com/nf-core/fetchngs/releases/tag/1.13.0
Please see the changelog: https://github.com/nf-core/fetchngs/releases/tag/1.13.0
Talk to the wet lab early.
Don’t assume the design is clean.
Ask:
What’s the hypothesis?
Are there replicates?
What are the controls?
Are the conditions randomized?
Good data starts long before you load the fastq.
Talk to the wet lab early.
Don’t assume the design is clean.
Ask:
What’s the hypothesis?
Are there replicates?
What are the controls?
Are the conditions randomized?
Good data starts long before you load the fastq.
Stop reprocessing FASTQ every time the annotation moves. Align once, query forever.
github.com/COMBINE-lab/gravlax
Stop reprocessing FASTQ every time the annotation moves. Align once, query forever.
github.com/COMBINE-lab/gravlax
Small enough to keep a whole cohort online instead of banishing reads to cold storage.
Small enough to keep a whole cohort online instead of banishing reads to cold storage.
But bioinformatics has its pain too.
A bad FASTQ file. Poor replicates. Missing metadata.
You can’t analyze what wasn’t measured right.
But bioinformatics has its pain too.
A bad FASTQ file. Poor replicates. Missing metadata.
You can’t analyze what wasn’t measured right.
Here you start letting the computer work for you.
Instead of:
fastqc sample1.fastq
fastqc sample2.fastq
fastqc sample3.fastq
You write:
for f in *.fastq; do fastqc $f; done
One command. All files.
This is the first taste of freedom.
Here you start letting the computer work for you.
Instead of:
fastqc sample1.fastq
fastqc sample2.fastq
fastqc sample3.fastq
You write:
for f in *.fastq; do fastqc $f; done
One command. All files.
This is the first taste of freedom.
From raw FASTQ files to differential expression, pathway enrichment, visualization, and biological interpretation, **Oxford OmicLine** helps researchers turn RNA-Seq datasets into reproducible scientific insights.
📊 **Analyze. Interpret. Discover.**
From raw FASTQ files to differential expression, pathway enrichment, visualization, and biological interpretation, **Oxford OmicLine** helps researchers turn RNA-Seq datasets into reproducible scientific insights.
📊 **Analyze. Interpret. Discover.**