Resources

Webinars

 
2021 International Smart Medical Forum
2021 International Smart Medical Forum

2021 智慧醫療及照護高峰論壇|跨域推進 智慧醫療再進化【Trend Forum】 October 15, 2021

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2021 Microsoft DevDays Asia
2021 Microsoft DevDays Asia

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2019 AI Infinity
2019 AI Infinity

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2021 International Smart Medical Forum
2021 International Smart Medical Forum

2021 智慧醫療及照護高峰論壇|跨域推進 智慧醫療再進化【Trend Forum】 October 15, 2021

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News

 

19 August 2022

Atgenomix is Now an HL7 Gold Member

As a Gold Member in Health Level Seven International (HL7), Atgenomix supports the HL7 objective to create a suite of standard-based technologies for streamlining sophisticated data management and computational analysis of biomedical and multi-omics information.

2 August 2022

Atgenomix Presents at Taiwan-Australia Collaboration Forum

Atgenomix CEO, Allen Chang, shared how our BioMed-IT platform can empower biotech and precision medicine industries to innovate at scale and speed.

1 August 2022

Atgenomix Receives Recognition from the 5th Charity Festival of Chinese

CSR2022 華人公益大使 recognizes the contributions of Atgenomix to the field of precision medicine.

16 May 2022

Atgenomix Staff Scientist Joins Virtual Symposium for Dentists

Yin-Hung Lin, Ph.D. presented and discussed how a unified bioinformatics platform can empower the precision medicine industry in the application of digital transformation to face the challenges of paradigm shift in dentistry and medicine, in particular oral cancer genomics.

1 April 2022

The Future of Precision Medicine

Allen joins Science Monthly as a guest contributor, sharing how biomedical information technology drives the future of precision medicine.

19 May 2020

Cloud-based genome analysis could help speed up development of a COVID-19 vaccine

Researchers in Taiwan gain access to a platform that processes genome sequencing data faster than conventional methods.

Collaborative Publications

 
 
ConnectedReads
ConnectedReads

Machine-learning optimized long-range genome analysis workflow for next-generation sequencing

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GraphSeq
GraphSeq

Accelerating String Graph Construction for De Novo Assembly on Spark

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SeqsLab
SeqsLab

An integrated platform for cohort-based annotation and interpretation of genetic variants on Spark

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Copy number variant
Copy number variant

Copy number variant hotspots in Han Taiwanese population induced pluripotent stem cell lines - lessons from establishing the Taiwan human disease iPSC Consortium Bank

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DeepVariant on Spark
DeepVariant on Spark

DeepVariant-on-Spark: Small-Scale Genome Analysis Using a Cloud-Based Computing Framework

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Rare mutations of two presynaptic cytomatrix genes
Rare mutations of two presynaptic cytomatrix genes

Identification of Rare Mutations of Two Presynaptic Cytomatrix Genes BSN and PCLO in Schizophrenia and Bipolar Disorder

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Novel nonsense homozygous mutation
Novel nonsense homozygous mutation

Identification of a novel nonsense homozygous mutation of LINS1 gene in two sisters with intellectual disability, schizophrenia, and anxiety

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Gene missense mutations
Gene missense mutations

Detection of Rare Methyl-CpG Binding Protein 2 Gene Missense Mutations in Patients with Schizophrenia

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Rare mutations of SCN9A, DPP4, ABCA13, and SYT14
Rare mutations of SCN9A, DPP4, ABCA13, and SYT14

Involvement of Rare Mutations of SCN9A, DPP4, ABCA13, and SYT14 in Schizophrenia and Bipolar Disorder

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