BioDiscovery, Inc.

Latest Nexus Copy Number Software Uses BAM MultiScale Reference Method
Software

Latest Nexus Copy Number Software Uses BAM MultiScale Reference Method

BioDiscovery’s Nexus Copy Number Software 10.0 is designed for integrated analysis of copy number, sequence variation and Loss of heterozygosity. The software derives quality copy number calls from whole exome, whole genome, shallow, targeted panel, and normal depth of coverage sequencing. Copy Number Software 10.0 comes with features such as user-specified event colors, export of distance...

Read More »
Services

New NxClinical 4.1 System allows combined analysis and interpretation of genomic variants.

BioDiscovery Inc.'s NxClinical 4.1 system is a software solution for the integration of copy number, sequence variants, and allelic changes obtained from microarray and NGS technologies. The updated software features trio analysis and support for single recessive inheritance tests and sequence variants tests, and now allows for the interpretation of genomic variants of any size. It also...

Read More »
NxClinical 4.0 Software features BAM MSR algorithm.
Software

NxClinical 4.0 Software features BAM MSR algorithm.

NxClinical 4.0 Software is used for analyses of copy number/allelic and sequence variant changes. Unit enables user to detect compound heterozygous event using interactive browser view. Software’s algorithm allows operator to derive copy number and allelic event changes from WES, WGS, targeted panels, and low pass sequencing data. Product offers interactive visualization tools which shows read...

Read More »
Software

Clinical Case Review Software improves process efficiency.

NxClinical handles every aspect of case review and reporting, from raw data to reports, in one enterprise-wide database system for clinical users. For process efficiency and quality, solution incorporates multi-user collaborative communication, audit-trail features, andÂ- automation capabilities. Decision support system utilizes user-specified rules for pre-classification of events. Other...

Read More »
Software

Cancer Genetics Expands BioDiscovery's Nexus Copy Number Platform to Identify Novel Biomarkers Predictive of Cancer Outcomes

Hawthorne, CA and Rutherford, NJ – Cancer Genetics, Inc. (Nasdaq: CGIX) and BioDiscovery, Inc. have announced expansion of the Nexus Copy Number Discovery platform in CGI research to uncover novel biomarkers which are predictive of cancer outcomes. Cancer Genetics has been able to leverage the Nexus Copy Number platform's unique ability to quickly digest large data sets to uncover correlations...

Read More »
Laboratory and Research Supplies and Equipment

N-of-One and BioDiscovery Partner to Deliver Tumor Genomics Analysis and Interpretation Platform

Partnership Equips Laboratories and Oncologists with a Foundation for Genomic Data Analysis through to Therapeutic Options Hawthorne, CA and Lexington, MA – BioDiscovery, Inc., a leader in DNA structural variant analysis laboratory software for copy number (CNV) and sequence variation, and N-of-One, the leading provider of molecular interpretation and therapeutic strategies for precision...

Read More »
Software

Data Analysis Software detects genomic aberrations.

Providing analysis of structural variation from CGH array, SNP array, and NGS platforms, Nexus Copy Number v7 supports small sequence variations, such as point mutations,Â- InDels, and inversions. Sequence variations can be interpreted alongside copy number changes for integrated view of genomic aberrations. This feature allows identification of mutations overlapping copy number...

Read More »
Services

BioDiscovery and AGRE Enter into a Co-Promotion Agreement

Hawthorne, CA, AND LOS ANGELES, CA - BioDiscovery, Inc. a leader in integrated software solutions for genomic-based research, and the Autism Genetic Resource Exchange (AGRE), a program of Autism Speaks, which collects and houses genetic and phenotypic data on over 1300 families with autism, have signed a co-promotion agreement. This agreement allows AGRE to provide copy number and allelic event...

Read More »
Software

Research Software provides gene expression analysis.

Supporting Affymetrix, Agilent, Illumina, and Roche NimbleGen array platforms, Nexus Expression v2 provides intuitive interface for using gene expression results to associate sample attributes with gene annotations and biological processes. With single mouse clicks, user can cluster genes and samples to discover expression patterns, simultaneously compare expression profiles of multiple...

Read More »
Services

Global Repository securely stores genomic variation data.

Accommodating high-demand requirements, Nexus DB provides secure off-site storage of data from Nexus Copy Number software to ensure 24/7 access to all information generated with automated backup and versioning control. Functionality also provides means to query results across multiple projects and facilitates collaborative work by enabling access to and review of data from anywhere in world by...

Read More »
Latest Nexus Copy Number Software Uses BAM MultiScale Reference Method
Software

Latest Nexus Copy Number Software Uses BAM MultiScale Reference Method

BioDiscovery’s Nexus Copy Number Software 10.0 is designed for integrated analysis of copy number, sequence variation and Loss of heterozygosity. The software derives quality copy number calls from whole exome, whole genome, shallow, targeted panel, and normal depth of coverage sequencing. Copy Number Software 10.0 comes with features such as user-specified event colors, export of distance...

Read More »
Services

New NxClinical 4.1 System allows combined analysis and interpretation of genomic variants.

BioDiscovery Inc.'s NxClinical 4.1 system is a software solution for the integration of copy number, sequence variants, and allelic changes obtained from microarray and NGS technologies. The updated software features trio analysis and support for single recessive inheritance tests and sequence variants tests, and now allows for the interpretation of genomic variants of any size. It also...

Read More »
NxClinical 4.0 Software features BAM MSR algorithm.
Software

NxClinical 4.0 Software features BAM MSR algorithm.

NxClinical 4.0 Software is used for analyses of copy number/allelic and sequence variant changes. Unit enables user to detect compound heterozygous event using interactive browser view. Software’s algorithm allows operator to derive copy number and allelic event changes from WES, WGS, targeted panels, and low pass sequencing data. Product offers interactive visualization tools which shows read...

Read More »
Software

Clinical Case Review Software improves process efficiency.

NxClinical handles every aspect of case review and reporting, from raw data to reports, in one enterprise-wide database system for clinical users. For process efficiency and quality, solution incorporates multi-user collaborative communication, audit-trail features, andÂ- automation capabilities. Decision support system utilizes user-specified rules for pre-classification of events. Other...

Read More »
Software

Cancer Genetics Expands BioDiscovery's Nexus Copy Number Platform to Identify Novel Biomarkers Predictive of Cancer Outcomes

Hawthorne, CA and Rutherford, NJ – Cancer Genetics, Inc. (Nasdaq: CGIX) and BioDiscovery, Inc. have announced expansion of the Nexus Copy Number Discovery platform in CGI research to uncover novel biomarkers which are predictive of cancer outcomes. Cancer Genetics has been able to leverage the Nexus Copy Number platform's unique ability to quickly digest large data sets to uncover correlations...

Read More »
Laboratory and Research Supplies and Equipment

N-of-One and BioDiscovery Partner to Deliver Tumor Genomics Analysis and Interpretation Platform

Partnership Equips Laboratories and Oncologists with a Foundation for Genomic Data Analysis through to Therapeutic Options Hawthorne, CA and Lexington, MA – BioDiscovery, Inc., a leader in DNA structural variant analysis laboratory software for copy number (CNV) and sequence variation, and N-of-One, the leading provider of molecular interpretation and therapeutic strategies for precision...

Read More »
Software

Data Analysis Software detects genomic aberrations.

Providing analysis of structural variation from CGH array, SNP array, and NGS platforms, Nexus Copy Number v7 supports small sequence variations, such as point mutations,Â- InDels, and inversions. Sequence variations can be interpreted alongside copy number changes for integrated view of genomic aberrations. This feature allows identification of mutations overlapping copy number...

Read More »
Services

BioDiscovery and AGRE Enter into a Co-Promotion Agreement

Hawthorne, CA, AND LOS ANGELES, CA - BioDiscovery, Inc. a leader in integrated software solutions for genomic-based research, and the Autism Genetic Resource Exchange (AGRE), a program of Autism Speaks, which collects and houses genetic and phenotypic data on over 1300 families with autism, have signed a co-promotion agreement. This agreement allows AGRE to provide copy number and allelic event...

Read More »
Software

Research Software provides gene expression analysis.

Supporting Affymetrix, Agilent, Illumina, and Roche NimbleGen array platforms, Nexus Expression v2 provides intuitive interface for using gene expression results to associate sample attributes with gene annotations and biological processes. With single mouse clicks, user can cluster genes and samples to discover expression patterns, simultaneously compare expression profiles of multiple...

Read More »
Services

Global Repository securely stores genomic variation data.

Accommodating high-demand requirements, Nexus DB provides secure off-site storage of data from Nexus Copy Number software to ensure 24/7 access to all information generated with automated backup and versioning control. Functionality also provides means to query results across multiple projects and facilitates collaborative work by enabling access to and review of data from anywhere in world by...

Read More »

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