Malcolm Moos

发表

Establishing reference samples for detection of somatic mutations and germline variants with NGS technologies

Hugo Y. K. Lam, Daoud M. Meerzaman, S. Sherry, 2019, bioRxiv.

Single-nucleus chromatin accessibility and RNA sequencing reveal impaired brain development in prenatally e-cigarette exposed neonatal rats

Zhongtian Chen, D. Xiao, Yong Li, 2022, iScience.

A multicenter study benchmarking single-cell RNA sequencing technologies using reference samples

W. Xiao, A. Farmer, M. Mehta, 2020, Nature Biotechnology.

A multi-center cross-platform single-cell RNA sequencing reference dataset

Wanqiu Chen, Andrew Farmer, Xin Chen, 2020, Scientific Data.

A Comprehensive Multi-Center Cross-platform Benchmarking Study of Single-cell RNA Sequencing Using Reference Samples

Wanqiu Chen, Andrew Farmer, Xiaojiang Xu, 2020, bioRxiv.

Current challenges and future directions for engineering extracellular vesicles for heart, lung, blood and sleep diseases

James E. Dahlman, Jennifer K. Lang, G. Vunjak‐Novakovic, 2023, Journal of extracellular vesicles.

Achieving robust somatic mutation detection with deep learning models derived from reference data sets of a cancer sample

Luis V. Santana-Quintero, W. Xiao, M. Mohiyuddin, 2022, Genome Biology.

Establishing community reference samples, data and call sets for benchmarking cancer mutation detection using whole-genome sequencing

Hugo Y. K. Lam, Winnie S. Liang, Daoud M. Meerzaman, 2021, Nature Biotechnology.

Toward best practice in cancer mutation detection with whole-genome and whole-exome sequencing

Thomas M. Blomquist, Daoud M. Meerzaman, S. Sherry, 2021, Nature Biotechnology.

Reproducible high yield sequencing of proteins electrophoretically separated and transferred to an inert support.

M. Moos, T. Liu, N. Nguyen, 1988, The Journal of biological chemistry.