Computational bio tool automates and standardizes genome sequencing analysis

In a single experiment, scientists can decipher the entire genomes of many patient samples, animal models, or cultured cells.
Medscape

Microarray-Based Prenatal Diagnosis for the Identification of Fetal Chromosome Abnormalities

JA Rosenfeld is an employee of Signature Genomic Laboratories, a subsidiary of PerkinElmer, Inc. The authors have no other relevant affiliations or financial involvement with any organization or ...
Labroots

Understanding Bioinformatics Workflows for NGS Analysis: Case Study with Whole-exome Sequencing Data

NGS enables the in-depth analysis of the genome and the identification and investigation of disease-associated variants–especially when workflows include target enrichment, which focuses on specific ...
Nanowerk

Third-Generation Sequencing in Genome Analysis

What is Third-Generation Sequencing? Third-generation sequencing, also known as long-read sequencing, refers to the latest advancements in DNA sequencing technologies that enable the analysis of ...