
Explore leveraging SNP arrays in cancer genomics beyond CNVs, focusing on mosaic gains/losses, HRD scores, and noninformative SNPs for improved diagnosis and treatment.

Explore chikungunya arthritis and dengue vascular permeability studies, focusing on translational science in arboviral pathogen research.

Explore the role of particle-associated bacteria in marine snow formation and its impact on the biological carbon pump in current and future ocean conditions.

Explore SARS-CoV-2 vaccine efficacy challenges, neutralizing antibody testing, and implications for booster shots using GenScript's surrogate virus neutralization test.

Explore global efforts in clinical genomics, from diagnosis to gene discovery. Learn about overcoming barriers and building infrastructure for integrating genomics into medical practice.

Explore NGS technologies' application in IVF, enhancing genetic screening and embryo selection for improved fertility outcomes.

Explore clinical NGS implementation at Holycross Cancer Center, focusing on challenges, solutions, and future directions in molecular diagnostics for cancer care.

Explore the versatility of Ion Torrent NGS systems for various applications, presented by Dr. Andy Felton, VP of Product Management & Market Development.

Explore molecular profiling of NSCLC samples using the Genexus turnkey NGS platform with Dr. Brendan Pang, a consultant pathologist and medical director.

Explore microfluidic vortex shedding for efficient cell engineering. Learn about Hydropore's intracellular delivery platform for rapid and gentle nucleic acid and gene editing complex delivery to various cell types.

Explore translational research strategies through RENACER example, enhancing impact of scientific discoveries in clinical settings.

Explore groundbreaking research on TRAIL's role in breast cancer metastasis, uncovering its function as a vascular gatekeeper and its therapeutic potential in preventing premetastatic niche formation.

Learn to translate human-readable genetic variation descriptions into unique computable variations using the Variation Normalizer tool for improved cancer genomics analysis and diagnosis.

Explore co-occurring driver mutations in lung adenocarcinoma, their impact on RAS signaling, and implications for targeted therapies. Gain insights into clinical cases and treatment strategies.

Explore epigenetic reprogramming in brain development pathways during non-small cell lung cancer metastasis. Gain insights into cutting-edge cancer genomics research and its implications for diagnosis and treatment.

Explore computational methods for predicting MHC anchor locations to enhance neoantigen identification and prioritization in cancer genomics, improving patient diagnosis and treatment.

Explore techniques for accurate somatic RNA variant calling in solid tumors, addressing key challenges and improving cancer genomics analysis.

Explore ATP-dependent chromatin remodeling, focusing on INO80's unique hexasome preference and its impact on higher-order chromatin organization. Gain insights into novel mechanisms regulating genome accessibility.

Explore the activation of retrotransposons in aging and neurodegeneration, focusing on LINE-1 elements' role in cellular senescence and potential implications for neurodegenerative diseases.

Explore how many-to-many protein networks function as versatile computational devices in multicellular organisms and their potential applications in synthetic biology for designing complex behaviors.

Explore DNA methylation in plants, its role in gene silencing, and CRISPR-based tools for targeted methylation changes in research and crop improvement.