Literature DB >> 29698836

System for Informatics in the Molecular Pathology Laboratory: An Open-Source End-to-End Solution for Next-Generation Sequencing Clinical Data Management.

Wenjun Kang1, Sabah Kadri2, Rutika Puranik2, Michelle N Wurst2, Sushant A Patil2, Ibro Mujacic2, Sonia Benhamed2, Nifang Niu2, Chao Jie Zhen2, Bekim Ameti2, Bradley C Long2, Filipo Galbo2, David Montes2, Crystal Iracheta2, Venessa L Gamboa2, Daisy Lopez2, Michael Yourshaw3, Carolyn A Lawrence3, Dara L Aisner3, Carrie Fitzpatrick2, Megan E McNerney4, Y Lynn Wang2, Jorge Andrade5, Samuel L Volchenboum5, Larissa V Furtado2, Lauren L Ritterhouse2, Jeremy P Segal6.   

Abstract

Next-generation sequencing (NGS) diagnostic assays increasingly are becoming the standard of care in oncology practice. As the scale of an NGS laboratory grows, management of these assays requires organizing large amounts of information, including patient data, laboratory processes, genomic data, as well as variant interpretation and reporting. Although several Laboratory Information Systems and/or Laboratory Information Management Systems are commercially available, they may not meet all of the needs of a given laboratory, in addition to being frequently cost-prohibitive. Herein, we present the System for Informatics in the Molecular Pathology Laboratory (SIMPL), a free and open-source Laboratory Information System/Laboratory Information Management System for academic and nonprofit molecular pathology NGS laboratories, developed at the Genomic and Molecular Pathology Division at the University of Chicago Medicine. SIMPL was designed as a modular end-to-end information system to handle all stages of the NGS laboratory workload from test order to reporting. We describe the features of SIMPL, its clinical validation at University of Chicago Medicine, and its installation and testing within a different academic center laboratory (University of Colorado), and we propose a platform for future community co-development and interlaboratory data sharing.
Copyright © 2018 American Society for Investigative Pathology and the Association for Molecular Pathology. Published by Elsevier Inc. All rights reserved.

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Year:  2018        PMID: 29698836      PMCID: PMC6039793          DOI: 10.1016/j.jmoldx.2018.03.008

Source DB:  PubMed          Journal:  J Mol Diagn        ISSN: 1525-1578            Impact factor:   5.568


  12 in total

1.  dbSNP: the NCBI database of genetic variation.

Authors:  S T Sherry; M H Ward; M Kholodov; J Baker; L Phan; E M Smigielski; K Sirotkin
Journal:  Nucleic Acids Res       Date:  2001-01-01       Impact factor: 16.971

2.  Clinical genomicist workstation.

Authors:  Mukesh K Sharma; Joshua Phillips; Saurabh Agarwal; Wesley S Wiggins; Savita Shrivastava; Sunita B Koul; Madhurima Bhattacharjee; Caerie D Houchins; Raghavendra R Kalakota; Bijoy George; Rekha R Meyer; David H Spencer; Christina M Lockwood; Tudung T Nguyen; Eric J Duncavage; Hussam Al-Kateb; Catherine E Cottrell; Suhasini Godala; Raviteja Lokineni; Sameer M Sawant; Vasudev Chatti; Suresh Surampudi; Raja Rao Sunkishala; Ramakant Darbha; Sharath Macharla; Jeffrey D Milbrandt; Herbert W Virgin; Robi D Mitra; Richard D Head; Shashikant Kulkarni; Andrew Bredemeyer; John D Pfeifer; Karen Seibert; Rakesh Nagarajan
Journal:  AMIA Jt Summits Transl Sci Proc       Date:  2013-03-18

3.  SeqReporter: automating next-generation sequencing result interpretation and reporting workflow in a clinical laboratory.

Authors:  Somak Roy; Mary Beth Durso; Abigail Wald; Yuri E Nikiforov; Marina N Nikiforova
Journal:  J Mol Diagn       Date:  2013-11-09       Impact factor: 5.568

4.  Clinical Validation of a Next-Generation Sequencing Genomic Oncology Panel via Cross-Platform Benchmarking against Established Amplicon Sequencing Assays.

Authors:  Sabah Kadri; Bradley C Long; Ibro Mujacic; Chao J Zhen; Michelle N Wurst; Shruti Sharma; Nadia McDonald; Nifang Niu; Sonia Benhamed; Jigyasa H Tuteja; Tanguy Y Seiwert; Kevin P White; Megan E McNerney; Carrie Fitzpatrick; Y Lynn Wang; Larissa V Furtado; Jeremy P Segal
Journal:  J Mol Diagn       Date:  2016-11-09       Impact factor: 5.568

5.  Memorial Sloan Kettering-Integrated Mutation Profiling of Actionable Cancer Targets (MSK-IMPACT): A Hybridization Capture-Based Next-Generation Sequencing Clinical Assay for Solid Tumor Molecular Oncology.

Authors:  Donavan T Cheng; Talia N Mitchell; Ahmet Zehir; Ronak H Shah; Ryma Benayed; Aijazuddin Syed; Raghu Chandramohan; Zhen Yu Liu; Helen H Won; Sasinya N Scott; A Rose Brannon; Catherine O'Reilly; Justyna Sadowska; Jacklyn Casanova; Angela Yannes; Jaclyn F Hechtman; Jinjuan Yao; Wei Song; Dara S Ross; Alifya Oultache; Snjezana Dogan; Laetitia Borsu; Meera Hameed; Khedoudja Nafa; Maria E Arcila; Marc Ladanyi; Michael F Berger
Journal:  J Mol Diagn       Date:  2015-03-20       Impact factor: 5.568

6.  The GeneInsight Suite: a platform to support laboratory and provider use of DNA-based genetic testing.

Authors:  Samuel J Aronson; Eugene H Clark; Lawrence J Babb; Samantha Baxter; Lisa M Farwell; Birgit H Funke; Amy Lovelette Hernandez; Victoria A Joshi; Elaine Lyon; Andrew R Parthum; Franklin J Russell; Matthew Varugheese; Thomas C Venman; Heidi L Rehm
Journal:  Hum Mutat       Date:  2011-03-22       Impact factor: 4.878

7.  AACR Project GENIE: Powering Precision Medicine through an International Consortium.

Authors: 
Journal:  Cancer Discov       Date:  2017-06-01       Impact factor: 39.397

8.  Validation and implementation of targeted capture and sequencing for the detection of actionable mutation, copy number variation, and gene rearrangement in clinical cancer specimens.

Authors:  Colin C Pritchard; Stephen J Salipante; Karen Koehler; Christina Smith; Sheena Scroggins; Brent Wood; David Wu; Ming K Lee; Suzanne Dintzis; Andrew Adey; Yajuan Liu; Keith D Eaton; Renato Martins; Kari Stricker; Kim A Margolin; Noah Hoffman; Jane E Churpek; Jonathan F Tait; Mary-Claire King; Tom Walsh
Journal:  J Mol Diagn       Date:  2013-11-02       Impact factor: 5.568

9.  COSMIC: mining complete cancer genomes in the Catalogue of Somatic Mutations in Cancer.

Authors:  Simon A Forbes; Nidhi Bindal; Sally Bamford; Charlotte Cole; Chai Yin Kok; David Beare; Mingming Jia; Rebecca Shepherd; Kenric Leung; Andrew Menzies; Jon W Teague; Peter J Campbell; Michael R Stratton; P Andrew Futreal
Journal:  Nucleic Acids Res       Date:  2010-10-15       Impact factor: 16.971

Review 10.  Next-Generation Sequencing in Oncology: Genetic Diagnosis, Risk Prediction and Cancer Classification.

Authors:  Rick Kamps; Rita D Brandão; Bianca J van den Bosch; Aimee D C Paulussen; Sofia Xanthoulea; Marinus J Blok; Andrea Romano
Journal:  Int J Mol Sci       Date:  2017-01-31       Impact factor: 5.923

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  3 in total

1.  Evaluation of Commercial Next-Generation Sequencing Bioinformatics Software Solutions.

Authors:  Rama R Gullapalli
Journal:  J Mol Diagn       Date:  2019-11-18       Impact factor: 5.568

Review 2.  A Genomic Information Management System for Maintaining Healthy Genomic States and Application of Genomic Big Data in Clinical Research.

Authors:  Jeong-An Gim
Journal:  Int J Mol Sci       Date:  2022-05-25       Impact factor: 6.208

3.  Development and validation of Houston Methodist Variant Viewer version 3: updates to our application for interpretation of next-generation sequencing data.

Authors:  Paul A Christensen; Sishir Subedi; Kristi Pepper; Heather L Hendrickson; Zejuan Li; Jessica S Thomas; S Wesley Long; Randall J Olsen
Journal:  JAMIA Open       Date:  2020-03-17
  3 in total

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