Sage Journals: Discover world-class research

Retricted access

Research article

First published 2003-06

DNA Sequence Evolution with Neighbor-Dependent Mutation

Peter F. Arndt, Christopher B. Burge, Terence Hwa

Journal of Computational Biology

Open access

Research article

First published 2015

Identification of Genetic Mutations in Human Lung Cancer by Targeted Sequencing

Hongxiang Feng, Xiaowei Wang, Zhenrong Zhang [...]

Cancer Informatics

Free access

Research article

First published 2013-3

Direct sequencing is a reliable assay with good clinical applicability for KRAS mutation testing in colorectal cancer

Jianfei Wang, Hongying Yang, Yinchen Shen [...]

Cancer Biomarkers

Open access

Research article

First published 2022

Migrating to Long-Read Sequencing for Clinical Routine BCR-ABL1 TKI Resistance Mutation Screening

Wesley Schaal, Adam Ameur, Ulla Olsson-Strömberg [...]

Cancer Informatics

Open access

Research article

First published 2016

Newborn Screening Quality Assurance Program for CFTR Mutation Detection and Gene Sequencing to Identify Cystic Fibrosis

Miyono M. Hendrix, Stephanie L. Foster, Suzanne K. Cordovado

Journal of Inborn Errors of Metabolism and Screening

Retricted access

Research article

First published 2020-2

Mutational Profile Using Next-Generation Sequencing May Aid in the Diagnosis and Treatment of Urachal Adenocarcinoma

Kristine M. Cornejo, Ediz F. Cosar, Gladell P. Paner [...]

International Journal of Surgical Pathology

Open access

Research article

First published 2022

Exploratory Data Analysis of Genomic Sequence of Variants of SARS-CoV-2 Reveals Sequence Divergence and Mutational Localization

Satyam Sangeet, Arshad Khan

Bioinformatics and Biology Insights

Free access

Research article

First published 2020-8

Identification of germline and somatic mutations in pancreatic adenosquamous carcinoma using whole exome sequencing

Hongyun Ma, Bin Song, Shiwei Guo [...]

Cancer Biomarkers

Open access

Research article

First published 2018-7

Identification of a low frequency missense mutation in MUC6 contributing to pulmonary artery hypertension by whole-exome sequencing

Lihui Zou, Wenqing Li, Jingli Han [...]

Pulmonary Circulation

Open access

Research article

First published 2020-9

Identification of a SCN4A mutation in a large Chinese family with atypical normokalemic periodic paralysis using whole-exome sequencing

XinYu Tan, SongNian Hu, Zongyu Xie [...]

Journal of International Medical Research

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