Agriculture MDPI’s Post

📍 The #1st paper of the #specialissue: "Gene Expression and Molecular Effects in Plants under Abiotic Stress" guest edited by Dr. Harshraj Shinde and Dr. Ulhas Sopanrao Kadam has been published! 🔎 Read more: https://lnkd.in/gh9SAu43 #abioticstress #cropplants #geneediting #genomics #transcriptomics #nextgenerationsequencing #plantphysiology #geneco_expressionanalysis #epigenetics #smallRNAs #genefamilies #molecularmarkers

Working on rare diseases? Our DECIPHER database gives you access to publicly available patient data allowing simple phenotypic and genotypic data comparisons. The latest DECIPHER database release covers a host of new features including: ➡️Integration of AlphaMissense scores from Google DeepMind to help you estimate how likely a nucleotide missense variant is to be pathogenic ➡️ Gene pages now link to the Open Targets Platform, facilitating the identification and prioritisation of potential therapeutic targets ➡️New Genome Aggregation Database (gnomAD v4.1) copy nucleotide variation (CNV) genome browser track displaying rare coding autosomal CNVs from exome sequencing of over 450,00 individuals Find out more here 👇 https://lnkd.in/eDFnQbCT #genetics #genomics #bioinformatics #raredisease

Our journey to 250k whole-genome sequences in the Alliance for Genomic Discovery continues as our eight partners now have access to over 86,000 sequences with associated clinical data. Watch the video below to hear from one of these partners in an exclusive interview with Iya Khalil, VP and Head of Data, A.I., and Genome Sciences at Merck. Learn more about how AGD can accelerate #drugdiscovery and shed light on the dark genome!  #healthcareinnovation #genomics #genetics #biobanking

Unlock the Secrets of Genomic Insights 🧬🔍 Join our 3-Day Certificate Online Training in NGS Data Analysis and Clinical Genetics Variant Analysis (ACMG-AMP). Master the tools and techniques essential for cutting-edge genetic research. Don't miss this opportunity to level up your skills and make a difference in the world of genetics! 🌍 DETAILS & REGISTRATION https://lnkd.in/g6WvKfR8 #bdglifesciences #VariantAnalysisTraining #GenomicAnalysis #Bioinformatics #NGS #DataAnalysis #VariantInterpretation #GenomicVariants #BioinformaticsTraining #Biotechnology #DataScience #variome #exome #genome #mutation #variantcalling #variantclassification #pathogenicvariant #benignvariant #cancergenetics #clinicalgenetics #genomics

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[NEW] Sporadic ALS involves an interplay between genetics & environment. Research now shows #epigenetic changes, specifically the DNA Methylome & formation of R-loops may be key parts of an epigenomic database to correlate these changes with the disease. ➡ https://bit.ly/3wxyp28 #epigenetics #cancerresearch #epigenomics #genomics #biomarkers

We wanted to remind you that our special Global Screening Array (GSA) 10% discount offer is coming to an end on Monday 17 June 2024. Our GSA service offers flexibility and affordability for population genetics, pharmacogenetics, disease studies and more, empowering researchers like you with expertly curated global content, providing insights that drive ground-breaking discoveries. Here's why our Illumina Infinium GSA stands out: 🔹 Flexible Solutions: Tailored to meet the diverse needs of genetic research, our GSA service offers flexibility in study design, sample types, and data analysis. 🔹 Affordable Innovation: We understand the importance of cost-effective solutions without compromising on quality. Our GSA service provides affordability without sacrificing accuracy or depth of data. 🔹 Expertly Curated Content: With curated content from around the globe, including diverse populations, our array ensures comprehensive coverage for a wide range of research applications. 🔹 Customisable booster content available. Whether you're exploring population genetics, investigating disease pathways, or delving into pharmacogenetics, our GSA service is your gateway to transformative insights. Are you ready to take your genetic research to the next level? Reach out to our team today to learn more about how our service can accelerate your research goals. 📧 [email protected] Promo Code: ARRAYS050524 #PopulationGenomics #GenomicsResearch #GeneticAnalysis #ResearchTools #ScienceDiscount #DiscoveriesAwait

#Introduction_of_bioinformatics_databases Part1 (Omim.org) OMIM, or Online Mendelian Inheritance in Man, is a comprehensive and authoritative database that catalogues human genes and genetic disorders. Created by Dr. Victor A. McKusick in 1966, OMIM provides a wealth of information on the genetic basis of inherited diseases, including detailed descriptions of gene function, clinical manifestations, and inheritance patterns. With over 25,000 entries, OMIM is an invaluable resource for researchers, clinicians, and students seeking to understand the genetic underpinnings of human health and disease. Whether you are studying a rare genetic disorder or exploring the role of a specific gene in a common disease, OMIM offers a wealth of knowledge to support your research efforts. #bioinformatics #biotechnology #gene #genetics #targetfinding

Variants of uncertain significance (VUS) for aHUS https://lnkd.in/echui7Kg Our article highlights a podcast by NHS England’s Helen Brittain, Clinical Lead for Rare Disease Diagnostics at Genomics England . #complement #aHUS #atypicalHUS #NHS #genetics #genome