Targeted next-generation sequencing of DNA has become more widely used in the management of patients with lung adenocarcinoma; however, no clear mitogenic driver alteration is found in some cases. Researchers at Memorial Sloan Kettering Cancer...
Read More »Palantir – characterization of cell fate probabilities in single-cell data
Single-cell RNA sequencing studies of differentiating systems have raised fundamental questions regarding the discrete versus continuous nature of both differentiation and cell fate. Researchers from Memorial Sloan Kettering Cancer Center present Palantir, an algorithm that models trajectories of differentiating cells ...
Read More »RNA-Seq reveals that widespread intronic polyadenylation inactivates tumour suppressor genes in leukaemia
DNA mutations are known cancer drivers. Memorial Sloan Kettering Cancer Center researchers investigated whether mRNA events that are upregulated in cancer can functionally mimic the outcome of...
Read More »RNA-Seq reveals widespread intronic polyadenylation diversifies immune cell transcriptomes
Alternative cleavage and polyadenylation (ApA) is known to alter untranslated region (3’UTR) length but can also recognize intronic polyadenylation (IpA) signals to generate transcripts that lose part or all of the coding region. Researchers from Memorial Sloan Kettering Cancer Center ...
Read More »Genome-wide profiling of the 3′ ends of polyadenylated RNAs
Alternative polyadenylation (APA) diversifies the 3′ termini of a majority of mRNAs in most eukaryotes, and is consequently inferred to have substantial consequences for the utilization of post-transcriptional regulatory mechanisms. Since conventional RNA-sequencing methods do not accurately define mRNA termini, ...
Read More »Enabling cross-study analysis of RNA-Sequencing data
Driven by the recent advances of next generation sequencing (NGS) technologies and an urgent need to decode complex human diseases, a multitude of large-scale studies were conducted recently that have resulted in an unprecedented volume of whole transcriptome sequencing (RNA-seq) ...
Read More »Foundation Medicine and Memorial Sloan Kettering Publish Validation Data for RNA Sequencing based FoundationOne® Heme Assay
CAMBRIDGE, Mass. & NEW YORK–(BUSINESS WIRE)–Foundation Medicine, Inc. (NASDAQ:FMI) and Memorial Sloan Kettering Cancer Center (MSK) today announced the publication of new, seminal data validating FoundationOne® Heme – the fully informative comprehensive genomic profiling assay for hematologic malignancies developed as ...
Read More »SplAdder – Identification, quantification and testing of alternative splicing events from RNA-Seq data
Understanding the occurrence and regulation of alternative splicing (AS) is a key task towards explaining the regulatory processes that help to shape the complex transcriptomes of higher eukaryotes. With the advent of high-throughput sequencing of RNA, the diversity of AS ...
Read More »Oqtans: The RNA-seq Workbench in the Cloud for Complete and Reproducible Quantitative Transcriptome Analysis
A team led by researchers at the Memorial Sloan-Kettering Cancer Center present Oqtans, an open-source workbench for quantitative transcriptome analysis, that is integrated in the Galaxy framework. Its distinguishing features include customizable computational workflows and a modular pipeline architecture that ...
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