OVARIE, PCOS clinic’s Post

Assessing the quality of gDNA is of utmost importance in NGS workflows. Long-read sequencing offers researchers the capability to analyze genomes more comprehensively and accurately. This webinar will provide an overview of the applications and key benefits of the Agilent Femto Pulse system particularly its use in PacBio long-read sequencing workflows. Register now: https://bit.ly/3UB3MkK #NGS #RNAseq #DNASequencing

If you're curious about adopting NGS as part of your research journey, but are perhaps a little intimidated by everything out there - then look no further than this webinar, "How to Plan Your First Sequencing Project". It couldn't be more clear! Take the (X)LEAP 😉

Did you know❓ NGS solutions can deliver complex variant detection in key genes like PMS2, BRCA, and APC, and a complete workflow that offers a real alternative to MLPA. Download the poster here: https://bit.ly/46YsP5w #TimeMatters #GenomicSequencing #InnovationInGenomics #DNAInsights #GenomicResearch #PrecisionMedicine #NGS #HereditaryCancer

Are phage libraries representative of the background B cell repertoire? We answer this question using our NGS-powered #antibody repertoire sequencing and analysis platform, Reptor. Find the answer in our most recent blog post, where we compare a VHH phage library to direct B cell sequencing from an immunized llama. https://lnkd.in/gQkk2jUY #antibodysequencing #antibodydiscovery

Unlock the power of 16S rRNA sequencing with the NEXTFLEX 16S V3-V4 Amplicon Seq Kit. Seamlessly analyze microbial communities and gain valuable insights into complex ecosystems. Elevate your research today! http://ms.spr.ly/6049iiSJN #NEXTFLEX #MicrobialAnalysis

Are you embarking on a new research project that involves sequencing? Schedule a complimentary Zoom session to explore Novogene America sequencing capabilities, including RNA seq, WGS, WES, Amplicon, Metagenomics, and more! Learn about how the NovaSeq X Plus can elevate your projects with efficiency, precision, all while staying within your budget constraints. Let's maximize the impact of your research endeavors together! #Novogene #Sequencing #NGS

Starting a new project that might need sequencing? I have availability next week for a free 30-minute consultation to chat about your project and explore the tailored sequencing services offered by Novogene America. Whether you require WGS, WES, mRNA seq, scRNA seq, metabolomics, metagenomics, or just want to know more about NGS, we've got the expertise and services to meet your sequencing needs. #NGS #nextgenerationsequencing #genomics #omics

Want to try Element Biosciences's new multi-omic platform? With our AVITI24™ Technology Access Program you can. This first access program allows you to send us your samples for pilot experiments to evaluate firsthand how AVITI24 can transform your research. AVITI24 Teton CytoProfiling enables analysis of RNA, proteins, and morphology in a single sample (over 1M cells). We’ll run and analyze the samples and provide you with data. Be the first to get hashtag #AVITI24 cytoprofiling data and get started today: https://bit.ly/3zV2zOq #aviti24 #multiomics #rnaseq #proteinexpression #pathwayanalysis #ngs #sequencing

Exome sequencing has an incremental diagnostic yield of 43% in cases of prenatally diagnosed agenesis of the corpus callosum following negative chromosomal microarray

BoltonLab (Ar)tifact Filtering (C)lonal (H)ematapoiesis Variant Calling Pipeline "This pipeline is designed to process mutant/wildtype H.sapiens sequencing data from Illumina based sequencing for low VAF CH variants. It features four variant callers (Mutect2, VarDictJava, Lofreq2, and Pindel) for variant detection and performs various false positive filters and detection methods (fp_filter, PoN Fisher’s Exact Test, XGB model, etc.). This pipeline also generates VEP style annotations for all called variants as well as additional putative driver annotations generated from various database sources (TOPMed, MSK-IMPACT, COSMIC, OncoKB, etc.)" #ClonalHematopoiesis #ClonalExpansion #bioinformatics #tools #CLI #bioinformaticstools https://lnkd.in/gchvXtRf