Open Journal of Genetics

Open Journal of Genetics

ISSN Print: 2162-4453
ISSN Online: 2162-4461
www.scirp.org/journal/ojgen
E-mail: ojgen@scirp.org
"Ultra-Fast Next Generation Human Genome Sequencing Data Processing Using DRAGENTM Bio-IT Processor for Precision Medicine"
written by Amit Goyal, Hyuk Jung Kwon, Kichan Lee, Reena Garg, Seon Young Yun, Yoon Hee Kim, Sunghoon Lee, Min Seob Lee,
published by Open Journal of Genetics, Vol.7 No.1, 2017
has been cited by the following article(s):
  • Google Scholar
  • CrossRef
[1] RawHash: Enabling Fast and Accurate Real-Time Analysis of Raw Nanopore Signals for Large Genomes
bioRxiv, 2023
[2] A Data Acquisition and Processing Method for Edge Computing Robotic Arm Behavior Recognition
… and Mobile Computing, 2022
[3] From molecules to genomic variations: Accelerating genome analysis via intelligent algorithms and architectures
Computational and …, 2022
[4] GenStore: a high-performance in-storage processing system for genome sequence analysis
Proceedings of the 27th …, 2022
[5] GenStore: A High-Performance and Energy-Efficient In-Storage Computing System for Genome Sequence Analysis
arXiv preprint arXiv …, 2022
[6] Going from molecules to genomic variations to scientific discovery: Intelligent algorithms and architectures for intelligent genome analysis
arXiv preprint arXiv …, 2022
[7] CSF-1 maintains pathogenic but not homeostatic myeloid cells in the central nervous system during autoimmune neuroinflammation
Proceedings of the …, 2022
[8] Effect of micro-osteoperforations on the gene expression profile of the periodontal ligament of orthodontically moved human teeth
Clinical Oral …, 2022
[9] SALoBa: Maximizing Data Locality and Workload Balance for Fast Sequence Alignment on GPUs
2022 IEEE …, 2022
[10] GenStore: In-Storage Filtering of Genomic Data for High-Performance and Energy-Efficient Genome Analysis
2022 IEEE Computer …, 2022
[11] GenPIP: In-Memory Acceleration of Genome Analysis via Tight Integration of Basecalling and Read Mapping
2022 55th IEEE/ACM …, 2022
[12] Genome sequencing of 320 Chinese children with epilepsy: a clinical and molecular study
Brain, 2021
[13] High performance of a GPU-accelerated variant calling tool in genome data analysis
bioRxiv, 2021
[14] Accelerating Genome Sequence Analysis via Efficient Hardware/Algorithm Co-Design
2021
[15] Hardware acceleration of genomics data analysis: challenges and opportunities
2021
[16] 联合氧化磷酸化缺陷 21 型 1 例报告并文献复习
临床儿科杂志, 2021
[17] Coding-complete genome sequences and mutation profiles of nine SARS-CoV-2 strains detected from COVID-19 patients in Bangladesh
2021
[18] Complexidade genética ea expressão da cor da pele, cor dos olhos e estatura humana: transposição didática
2020
[19] A Bioinformatics Crash Course for Interpreting Genomics Data
2020
[20] Justice in the Genomic and Digital Era: A Different World Requiring Different Law
2020
[21] Targeting CSF-1 ameliorates experimental autoimmune encephalomyelitis by depleting inflammatory monocytes and microglia in the central nervous system without …
2020
[22] Autophagy mitigates ethanol-induced mitochondrial dysfunction and oxidative stress in esophageal keratinocytes
2020
[23] Neuroinflammation and EIF2 Signaling Persist despite Antiretroviral Treatment in an hiPSC Tri-culture Model of HIV Infection
2020
[24] Big data in biology: The hope and present-day challenges in it
2020
[25] Modeling Complex Neurological Disorders with Human Induced Pluripotent Stem Cells
2020
[26] Accelerating Genome Analysis: A Primer on an Ongoing Journey
2020
[27] Neuroinflammation and EIF2 signaling persist in an HiPSC tri-culture model of HIV infection despite antiretroviral treatment
2019
[28] Advanced Whole Genome Sequencing Using a Complete PCR-free Massively Parallel Sequencing (MPS) Workflow
2019
[29] Genetic Data Misuse: Risk to Fundamental Human Rights in Developed Economies
2019
[30] Managing genomic variant calling workflows with Swift/T
2019
[31] Advanced Whole Genome Sequencing Using an Entirely PCR-free Massively Parallel Sequencing Workflow
bioRxiv, 2019
[32] Review of Applications of High-Throughput Sequencing in Personalised Medicine: Barriers and Facilitators of Future Progress in Research and Clinical Application
2018
[33] New literacy challenge for the twenty-first century: genetic knowledge is poor even among well educated
Journal of Community Genetics, 2018
[34] Review of applications of high-throughput sequencing in personalized medicine: barriers and facilitators of future progress in research and clinical application
2018
[35] NGSOne: 클라우드 기반의 유전체 (NGS) 데이터 분석 툴
2018
[36] NGSOne: Cloud-based NGS data analysis tool
2018
[37] Nathaniel P. Sotuyo, 2 Eugene Mironets, Kieona Cook, 2 Hakon Hakonarson, 6, 7 Stewart A. Anderson, 2, 3,* and Kelly L. Jordan-Sciutto
Free SCIRP Newsletters
Copyright © 2006-2024 Scientific Research Publishing Inc. All Rights Reserved.
Top