Top Tweets for #VariantCalling
Alignment formats store where reads map on a reference genome.
SAM is human readable but large.
BAM is compressed and indexed for efficient analysis.
CRAM is even smaller and uses the reference genome for compression.
#RNAseq #VariantCalling #GenomicsData #NGSanalysis
New study demonstrates up to 73% reduction in genome analysis errors using AI-trained models versus standard approaches
https://t.co/Bo82RdGuom
#Genomics #WholeGenomeSequencing #VariantCalling #AIinGenomics
#DeepVariant #Pangenome #DNBSEQT7plus #NGS
Register here - https://t.co/i4OT8I9Vv2
Check reviews here - https://t.co/Vl7C5Ld0fq
The most comprehensive NGS fundamentals and Data Analysis (Linux) workshop
#NGS #DNASeq #VariantCalling #Anconda #Conda #Linux #fastq #fastqc #trimmomatic #BWA #sam #bam #vcf #illumina #Iontorrent #nanopore #Sequel #SMRT
أهلاً بيكم في حلقة جديدة من "سلسلة الأدوات البحثية" 🧬🤍
النهارده هنتكلم عن أداة تقيلة شوية 👀
✨ GATK — العمود الفقري لتحليل الطفرات الجينية ✨
https://t.co/HAiSMKsQxp
👍🪄
#بوصلتك_للعلوم
#Bioinformatics
#GATK
#NGS
#VariantCalling
#Genomics
@medrxivpreprint on early access data generated by Baylor College of Medicine scientists with @illumina Constellation Mapped Read Technology. #genomics #VariantCalling #DRAGEN #Constellation https://t.co/VjmvERjMWS
Combine both short- and long-read data in one workflow with @sentieon pangenome pipelines. Donald Freed & Theresa Wohlever will show attendees how to leverage the latest variant calling techniques: https://t.co/hGyHjXvMfL
#WGS #Genomics #VariantCalling
Accurate somatic small variant discovery for multiple sequencing technologies with DeepSomatic. #SomaticVariants #ShortReads #LongReads #VariantCalling #Genomics #Bioinformatics #ToolsBenchmarking #ReferenceDatasets @NatureBiotech
https://t.co/a7cngfPMTM
Successfully ran a variant calling analysis of the 2014 Ebola Virus strain against its 1972 Reference Genome using a single VCF command in the pipeline.
#Bioinformatics #Ebola #VariantCalling #Genomics
Remove reference bias & improve variant calling accuracy by combining both short- and long-read data. Learn how to leverage @sentieon pangenome pipelines from Donald Freed & Theresa Wohlever: https://t.co/9Db96uOJa2
#WGS #Genomics #VariantCalling
Learning-based parallel acceleration for HaplotypeCaller. #VariantCalling #HaplotypeCaller #GATK #Genomics #Bioinformatics #BMCbioinformatics
https://t.co/L0fN9LSVDu
BREAKTHROUGH DISCOVERY
🚨 BREAKTHROUGH 🚨 Our #Hangdjinn engine just uncovered hidden genomic anomalies in #BRAFmutant cancer that completely escape conventional #variantcalling!
🔬 Using real chr7 + COLO829 data, we discovered 4 biologically coherent regions with:
• Alu insertions (+26% GC)
• Microsatellite instability
• CpG island aberrations
• Complex k-mer shifts
Something extraordinary happens when advanced computational analysis meets cancer genomics! 🧬
#CancerResearch #Genomics #Bioinformatics #DNAanalysis
🚀New Blog Post!
Just finished a training project on variant calling using zebrafish data from @UofGlasgow study on fisheries selection (PRJNA630223)
Walked through the full pipeline: QC → alignment → variant calling → VEP annotation
#Genomics #Zebrafish #VariantCalling
#NGS #Workshop #update #upskill #Get2025ResearchReady
For Course details & Registration - https://t.co/IAseu1zHsk
Check live reviews - https://t.co/B76I0V5E98
#bioinformatics #ngs #dna #dnaseq #fastqc #trimmomatic #bwa #bowtie #variantcalling #sam #bam #cigar #multiqc #vcf #snp
🚨 NEW RESEARCH! ⚕️ 🩺
Bollas et al. introduce VarRNA, a novel classifier of single nucleotide variants and insertions/deletions from tumor transcriptomes using RNA-seq data.
https://t.co/fJgSqCV1nM
#RNAseq #VariantCalling
ICYMI: Manual #variantcalling workflows can’t keep up anymore. We’ve seen a surge in requests from #biotech companies needing scalable, automated #bioinformatics #pipelines to make sense of their #genomic data. Read more: https://t.co/i5c6yCJH23 #genomics #precisionmedicine #NGS
Fast-Track Genomics Sunday at BIB!
Learn. Practice. Master.
📅 Date: Sunday, 15th June 2025
📍 Where: Online | Live + Self-paced Practical
Register Now! https://t.co/FYKPxLi9TH
COST: 500/- for each module
#BioinformaticsTraining #NGSAnalysis #VariantCalling
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