Blogs Archive - Page 3 of 15

A first-of-its-kind clinical research genetics knowledgebase – Accelerate your case review with N_xClinical

Impact | 2021-12-16

Genetic disease

Oncology

Technology development

NxClinical Software

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Hello, ACMG scoreboard. Goodbye, external calculator tools

Impact | 2021-10-06

Cytogenomics

Genetic disease

Molecular genomics

Technology development

NxClinical Software

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The DGV score and so much more

Impact | 2021-09-02

Cytogenomics

Genetic disease

Molecular genomics

NxClinical Software

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Maximize Clinical Research Data With BioDiscovery’s Genomics AI-Enabled Software Solution

2021-08-16

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Lucky No. 14 – ACMG adds new genes for reporting secondary findings

Education | 2021-06-02

Genetic disease

Molecular genomics

NxClinical Software

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Publication notes superiority of N_xClinical software for CNV detection from low pass sequencing

Impact | 2020-05-13

Cytogenomics

Genetic disease

Molecular genomics

Technology development

NxClinical Software

Read Blog

Aberrant Cell Fraction Estimation in N_xClinical 5.0

Education | 2019-07-09

Genetic disease

Oncology

Solid tumors

Technology development

NxClinical Software

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Recent publications illustrate the wide applicability of BioDiscovery’s CNV from NGS algorithm

2019-04-18

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Copy Number and Loss of Heterozygosity Analysis in Tumors

Education | 2019-02-02

Oncology

Solid tumors

NxClinical Software

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OMIM data in NxClinical

Education | 2018-09-20

Genetic disease

Technology development

NxClinical Software

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Significant Cost Savings with Single NGS Test vs. Other Strategies

2018-07-19

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Trio analysis in N_xClinical – Heritable retinal dystrophies in the Costa Rican population Case Study

2018-05-02

NxClinical Software

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Clinical Conversation – Ingrid Simonic: Optimizing and Consolidating Multiple Testing Strategies to Increase Efficiency with Increasing Testing Demand

2018-04-30

NxClinical Software

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N_xClinical February track updates

2018-02-16

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How are systematic correction files used for correcting probe values?

2017-12-06

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Blog

Copy Number and AOH Detection from Next-Generation Sequencing

A first-of-its-kind clinical research genetics knowledgebase – Accelerate your case review with N_xClinical

Hello, ACMG scoreboard. Goodbye, external calculator tools

The DGV score and so much more

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Maximize Clinical Research Data With BioDiscovery’s Genomics AI-Enabled Software Solution

Lucky No. 14 – ACMG adds new genes for reporting secondary findings

Publication notes superiority of N_xClinical software for CNV detection from low pass sequencing

Aberrant Cell Fraction Estimation in N_xClinical 5.0

Recent publications illustrate the wide applicability of BioDiscovery’s CNV from NGS algorithm

Copy Number and Loss of Heterozygosity Analysis in Tumors

OMIM data in NxClinical

Significant Cost Savings with Single NGS Test vs. Other Strategies

Trio analysis in N_xClinical – Heritable retinal dystrophies in the Costa Rican population Case Study

Clinical Conversation – Ingrid Simonic: Optimizing and Consolidating Multiple Testing Strategies to Increase Efficiency with Increasing Testing Demand

N_xClinical February track updates

How are systematic correction files used for correcting probe values?

Stay up-to-date on cutting-edge genetic analysis. Subscribe to our newsletter.

Optical Genome Mapping

Software

Nucleic Acid Purification

Data Services

Focus Areas

Applications

Learn

Library

Blog

Copy Number and AOH Detection from Next-Generation Sequencing

A first-of-its-kind clinical research genetics knowledgebase – Accelerate your case review with NxClinical

Hello, ACMG scoreboard. Goodbye, external calculator tools

The DGV score and so much more

Search

Displaying {results_count} results of {results_count_total} for {phrase}

Displaying {results_count} results of {results_count_total}

Topic

Application

Product

All Blogs

Maximize Clinical Research Data With BioDiscovery’s Genomics AI-Enabled Software Solution

Lucky No. 14 – ACMG adds new genes for reporting secondary findings

Publication notes superiority of NxClinical software for CNV detection from low pass sequencing

Aberrant Cell Fraction Estimation in NxClinical 5.0

Recent publications illustrate the wide applicability of BioDiscovery’s CNV from NGS algorithm

Copy Number and Loss of Heterozygosity Analysis in Tumors

OMIM data in NxClinical

Significant Cost Savings with Single NGS Test vs. Other Strategies

Trio analysis in NxClinical – Heritable retinal dystrophies in the Costa Rican population Case Study

Clinical Conversation – Ingrid Simonic: Optimizing and Consolidating Multiple Testing Strategies to Increase Efficiency with Increasing Testing Demand

NxClinical February track updates

How are systematic correction files used for correcting probe values?

Stay up-to-date on cutting-edge genetic analysis. Subscribe to our newsletter.

A first-of-its-kind clinical research genetics knowledgebase – Accelerate your case review with N_xClinical

Publication notes superiority of N_xClinical software for CNV detection from low pass sequencing

Aberrant Cell Fraction Estimation in N_xClinical 5.0

Trio analysis in N_xClinical – Heritable retinal dystrophies in the Costa Rican population Case Study

N_xClinical February track updates