Top Tweets for #VariantAnnotation
AdaGenes: A streaming processor for high-throughput annotation and filtering of sequence variant data. #GeneticVariants #VariantFiltering #VariantAnnotation #VCFs #Genomics #Bioinformatics @biorxiv_bioinfo
https://t.co/cp24x9gt1f
FAVOR-GPT: A generative Natural Language Interface to Whole Genome Variant Functional Annotations. #WGS #WES #VariantAnnotation #LLMs @BioinfoAdv
https://t.co/xMTiMOLsCc
📢 NGS – Genome Variant Analysis
👉 5-6 September 2024
💻 Streamed
#bioinformatics #training @isbsib #NGS #VariantCalling #VariantAnnotation #GermlineMutations
🚨 Apply at https://t.co/urov8OMu6J
Whether you are an experienced user or brand new to Alamut™ Visual Plus, this new technical note will help you navigate variant analysis with ease.
Get it now: https://t.co/hIGXuS1IJT
#variantanalysis #genomics #NGS #variantannotation #bioinformatics
Whether you are an experienced user or brand new to Alamut™ Visual Plus, our new technical note will help you navigate variant analysis with ease.
Get it now: https://t.co/hIGXuS1IJT
#variantanalysis #genomics #NGS #variantannotation #bioinformatics
Discover how Alamut™ Visual Plus implements nomenclature guidelines to enhance accurate variant analysis.
Download your technical note now: https://t.co/hIGXuRK7lj
#variantanalysis #genomics #NGS #variantannotation #bioinformatics
FAVOR: Functional Annotation of Variants Online Resource and Annotator for Variation across the Human Genome. #VariantAnnotation #HumanGenome #WebTool @biorxivpreprint https://t.co/LIqnkBIH36
Annotation Query (AnnoQ): an integrated and interactive platform for large-scale genetic variant annotation. #VariantAnnotation #Bioinformatics https://t.co/G2qRF2FA9l @NAR_Open
STAAR Workflow: A cloud-based workflow for scalable and reproducible rare variant analysis. #VariantAnalysis #WDL #VariantAnnotation https://t.co/xKzBl60ifF #Bioinformatics
Annotating and prioritising genomic variants using the Ensembl Variant Effect Predictor ‐ a tutorial. #GenomicVariants #VariantAnnotation #VariantPrioritisation #VEP #Tutorial https://t.co/SQyt65OMjB #HumanMutation
utr.annotation: a tool for annotating genomic variants that could influence post-transcriptional regulation. #UTRs #VariantAnnotation https://t.co/i45DkLfqFQ #Bioinformatics
Cruxome: a powerful tool for annotating, interpreting and reporting genetic variants. #SNV #INDELS #VariantAnnotation
https://t.co/D5128tC6dM #BMCgenomics
Join me, folks from DNAnexus, CMU Libraries, Google Health, Kings College London, and many other places for a virtual MultiOmics Clinical Reporting Hackathon June 1-4! https://t.co/5OVyYAJZhb
#rnaseq #structuralvariants #TCRs #polygenicriskscores #variantannotation #OMOP #FHIR
iVar, an Interpretation-Oriented Tool to Manage the Update and Revision of Variant Annotation and Classification
#NGS #VariantAnnotation #DataManagement #ClinicalGenomics
https://t.co/Fj7pVkNohy @MDPIOpenAccess
Interested in #genomicanalysis #DNAsequencing #RNAseq #variantAnnotation ? Join @WestGrid, @UBC & @BCCHF in June! https://t.co/OwbaYUBYW3
Get up-to-date variant annotations via our easy2use #python client. http://t.co/68X5Hvtrpn #bioinformatics #variantannotation
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