Breakthroughs in Diagnosing Colorectal Cancer with Rare Genetic Variants
A new study emphasizes the potential of advanced sequencing techniques in improving outcomes for CRC patients with rare genetic variants.
A new study emphasizes the potential of advanced sequencing techniques in improving outcomes for CRC patients with rare genetic variants.
The collaboration seeks to demonstrate the value of WGS as a first-line genetic test for postnatal diagnosis of developmental delay disorders.
Illumina's Global Health Access Initiative will support access to pathogen sequencing tools for public health in lower income countries.
New Element Biosciences technology has helped identify the likely genetic causes of disorders in six of nine children from Sonora, Mexico.
Read MoreThe new DM-Seq technique allows for scientists to profile DNA using very small samples and without damaging the sample.
Read MoreThe noninvasive method diagnoses atopic dermatitis by analyzing RNA from samples of sebum collected from infants using an oil-blotting film.
Read MoreUsing a CRISPR-based depletion technology and NGS overcomes limitations by targeting and removing abundant host and microbial rRNA sequences, making NGS suitable for pandemic preparedness.
Read MoreThe study’s multi-cancer early detection data show Exai’s RNA- and AI-based platform can detect multiple cancer types at the earliest stages using a single, standard blood sample.
Read MoreMetagenomic sequencing offers actionable antimicrobial resistance predictions for bloodstream infections faster than conventional lab tests.
Read MoreCentogene launched an enhanced next-generation sequencing (NGS)-based assay, for rare and neurodegenerative diseases.
Read MorePCR Biosystems launched a new proofreading polymerase mix for NGS library preparation workflows: the VeriFi Library Amplification Mix.
Read MoreBio-Rad Laboratories launched two new thermal cyclers, designed to optimize PCR applications such as sequencing, cloning, and genotyping.
Read MoreTo create the new assay, Acutis Diagnostics will pair SOPHiA DDM for Hereditary Cancers Solution with their laboratory analysis technologies.
Read MoreThough not a new diagnostic technique, multiplex testing is poised to become the standard of diagnostic care in the post-pandemic world.Â
Read MoreTecan and Element Biosciences are collaborating to offer an improved benchtop NGS workflow with MagicPrep NGS and the AVITI System.
Read MoreTecan has partnered with Singular Genomics to use its turnkey MagicPrep NGS system to help create sequencing-ready libraries.
Read MoreBio-Rad Labs is showcasing compatibility of its SEQuoia RNA library preparation kits with new innovative sequencers.
Read MoreThermo Fisher Scientific launched its Applied Biosystems TaqPath Seq HIV-1 Genotyping Kit, an assay that examines positive samples of HIV.
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