🧬 Master the NGS Pipeline! Join our 6-week program “From Sample to Sequencer: A Practical Guide to NGS Workflows” bridging wet-lab protocols & bioinformatics. 🔗 Register here for curriculum & details: forms.gle/SMexf9AGnvbNAGpy8 #NGS #Genomics #Bioinformatics #VariantAnalysis

Scientists and AI agents can co‑pilot medical science, together. AIPOCH.com Aipoch is the first contact: the first @OpenClaw‑integrated medical science AI network. What you can do with Aipoch: Run medical science workflows (papers → hypotheses → protocols → analysis) Build, share, and use open‑source med‑science skills with a community If you’re building in med‑AI, plug in with us. #OpenClaw #AgentBots #AISkills #MedScience #Genomics #AIPOCH #VariantAnalysis #FutureOfMed

Vulnerabilities don’t often exist in isolation, yet many researchers only chase new bugs and ignore the ground already explored. If a developer made a mistake in their code that caused a vulnerability, they likely made that mistake elsewhere in the codebase, too. In a rush to patch one bug, developers may also fail to perform deeper root cause analysis of WHY that vulnerability occurred, and fail to build secure guardrails to prevent future occurrences. These factors can give rise to a surprisingly rich source of vulnerabilities and facilitate a less resource-intensive approach to vulnerability research. Here are 3 high-impact areas to focus on: 💥 Variants 💥  A particular code pattern that caused a vulnerability exists elsewhere in the code, creating more vulnerabilities. 💥 Insufficient patches 💥  A patch for a vulnerability does not adequately resolve the root cause, leaving various bypasses available for the vulnerability to still be exploited. 💥 Regression 💥  A vulnerability is patched in the code but, due to lack of regression testing or secure guardrails, is revived when future changes in the code weaken or remove the patch. These aren’t theoretical either. They’ve led to multiple CVEs in real projects like libexpat! Want to learn how to turn CVE writeups into your next bug report? All this and much more is covered in Chapter 3 of From Day Zero to Zero Day! Get your copy now 👇 📘 Amazon: amazon.com/Day-Zero/dp/17185… 📘 No Starch: nostarch.com/zero-day 📕 Barnes & Noble: barnesandnoble.com/w/from-da… #BugBounty #AppSec #VariantAnalysis #CyberSecurity #CodeReview

PanVA: a visual analytics tool for pangenomic variant analysis. #Pangenomes #VariantAnalysis #DataVisualization #Genomics #Bioinformatics @biorxiv_bioinfo biorxiv.org/content/10.1101/…

New Feature Alert! Phased variants can be a challenge, but our latest blog covers how to collapse phased variants in VarSeq like a pro! Learn more here: bit.ly/47orIh7 #Genomics #NGS #RareDisease #VarSeq #PhasedVariants #VariantAnalysis #PrecisionMedicine

Our webinar, "Hereditary Cancer: Taking on Tomorrow with Powerful Insights," is starting now. Tune in live or on-demand here: hubs.la/Q02PhT3_0 #NGS #variantanalysis

Mahindra Scorpio N is currently one of India's most popular full-size SUVs under a Rs 25 lakh price tag. The Scorpio N comes with a starting price of Rs 13.85 lakh (ex-showroom) and is available in 6 variants. The Scorpio N is one of the most affordable 4X4 full-size SUVs that one can buy in the country. Swipe right for the full detailed analysis- shorturl.at/90GO6 . . . #mahindrascorpio #mahindracars #scorpio #scorpioN #variantanalysis #91wheels

Analysis of 10,478 cancer genomes identifies candidate driver genes and opportunities for precision oncology. #CancerGenomes #CancerDriverGenes #WGS #VariantAnalysis #PrecisionOncology #Genomics #Bioinformatics @NatureGenet nature.com/articles/s41588-0…

Name badges ready for #veptc2023! #ClinicalGenetics with real examples. Your last chance for virtual reg! ✅hands-on workshops 2-4 Oct 📅 BCN Hybrid 💻 organised by @humangenomeorg & @cnag_eu @PCB_UB 👉veptc.variome.org #genomics #genomic #variantanalysis #Genetics

bamSliceR: cross-cohort variant and allelic bias analysis for rare variants and rare diseases. #VariantAnalysis #RareDiseases @biorxivpreprint biorxiv.org/content/10.1101/…

Come learn about #NGS #variants in #ClinicalGenetics with real examples. Your last chance for virtual reg! 2-4 Oct 📅 BCN Hybrid 💻 organised by @humangenomeorg & @cnag_eu @PCB_UB 👉veptc.variome.org #genomics #genomic #variantanalysis #genetic

Acorn: an R package for de novo variant analysis. #VariantAnalysis #Bioinformatics @BMCBioinfo bmcbioinformatics.biomedcent…

but he was eating around it! My read on this was: he didn't actually complain (and claims to not have been visibly upset). It's just that, when she saw he was eating just the chocolate part, she asked if he doesn't like the cake.

oh

oh

Scalable and efficient DNA sequencing analysis on different compute infrastructures aiding variant discovery #VariantAnalysis #NfCore #Sarek @biorxivpreprint biorxiv.org/content/10.1101/…

welllllllllllllll yes I do wonder if the women have just as many stories, but they don't want to say "I'm good at sex" on twitter for many reasons

I'm noticing a lot of these compliments are people being complimented by women about their sexual prowess

ill fix it soon

me