Clint Valentine (@clintcodesbio) 's Twitter Profile
Clint Valentine

@clintcodesbio

All things bioinformatics at Fulcrum Genomics

ID: 2766406302

linkhttp://github.com/clintval calendar_today25-08-2014 13:58:22

2,2K Tweet

729 Followers

948 Following

Ultima Genomics (@ultimagenomics) 's Twitter Profile Photo

We are excited to launch the UG 100™ with substantial improvements in indel accuracy, achieving a 99.4% INDEL F1 score and unveiling our new ppmSeq™ technology, capable of achieving 1 in 1,000,000 raw read error rates for SNVs, or Q60-level precision. businesswire.com/news/home/2024…

We are excited to launch the UG 100™ with substantial improvements in indel accuracy, achieving a 99.4% INDEL F1 score and unveiling our new ppmSeq™ technology, capable of achieving 1 in 1,000,000 raw read error rates for SNVs, or Q60-level precision.

businesswire.com/news/home/2024…
Nils Homer (@nilshomer) 's Twitter Profile Photo

The theme of #AGBT24 so far has been amazing molecular biology and technological innovations that solve problems previously requiring #Bioinformatics solutions.

Clint Valentine (@clintcodesbio) 's Twitter Profile Photo

10x can't possibly sue Singular over spatial sequencing since Singular's doing spacial (outer space!) sequencing instead. Heavy coin too. Maybe I got an ultra-rare misprint? #AGBT

10x can't possibly sue Singular over spatial sequencing since Singular's doing spacial (outer space!) sequencing instead. Heavy coin too. Maybe I got an ultra-rare misprint? #AGBT
Matthew Parker (@bioinfomatt) 's Twitter Profile Photo

A key skill in bioinfo is assessment of raw seq data. Tools like IGV are useful to view aligned reads & variants. I've manually reviewed 1000s of variants and it's worth knowing what a real variant looks like! From Sirisha in the Oxford Nanopore #EPI2ME team: labs.epi2me.io/reviewing-bam

Chris Miller (@chrisamiller) 's Twitter Profile Photo

Two other resources of note for IGV: - Interactive guide to getting started with IGV: sandbox.bio/tutorials/igv-… - The supplement to this article, which is an incredibly comprehensive visual guide to reviewing somatic variants: ncbi.nlm.nih.gov/pmc/articles/P…

Clint Valentine (@clintcodesbio) 's Twitter Profile Photo

This is a remarkable and necessary tool for the Nextflow community. So excited to see the developer experience get better! Now we can stop worrying about code style and get to workflow-making!

Pierre Marijon 🏳️‍🌈 (@pierre_marijon) 's Twitter Profile Photo

Hello to all #bioinformatics #rustlang, I often copy code to generate data when writing tests. After 3 or 4 times, I got fed up and created biotest crates. biotest can generate fasta, fastq and vcf, I'm open to any suggestion, feedback or contribution. github.com/natir/biotest

Hello to all #bioinformatics #rustlang,

I often copy code to generate data when writing tests. After 3 or 4 times, I got fed up and created biotest crates.

biotest can generate fasta, fastq and vcf, I'm open to any suggestion, feedback or contribution.

github.com/natir/biotest