DISCOVER GOLDEN HELIX ANALYTIC SOLUTIONS

  • SNP ANALYSIS
  • CNV ANALYSIS
  • DNA-SEQ ANALYSIS
  • SVS CORE PLUS
  • ANALYTIC SERVICES

Learn more about
SNP Analysis »

SNP Analysis

With support for both case-control and quantitative traits, candidate genes or whole genome data, the SNP Analysis Package delivers a broad array of workflows for quickly and easily identifying SNPs associated with disease or other phenotypes. Functionality encompasses the breadth of the SNP analysis pipeline from quality assurance and genotype association testing to linkage disequilibrium and haplotype analysis.

Learn more about
Copy Number Analysis »

CNV Analysis

The CNV Analysis Package offers a complete set of tools for identifying and assessing the significance of copy number variations from microarray or aCGH data. Included is the ability to process raw intensities, identify break points in log ratio data, perform association or regression on a variety of covariates, and visually compare copy number variations between two or more sample groups in a variety of plots.

Learn more about
DNA-Seq Analysis »

DNA-Seq Analysis Package

The DNA-Seq Analysis Package delivers the latest tertiary analysis methods for rare and common variants enabling quick and easy identification of causal variants from next-generation sequencing data. General workflows include the ability to rapidly filter massive data sets by any genomic region, annotation, or quality score, perform collapsing and association methods to assess rare variant burden, and run variant classification to understand potential downstream effects of variants.

Learn more about
SVS Core Plus »

SVS Core Plus

SVS Core Plus is the foundational package of SVS. It offers a robust platform for efficiently managing, manipulating, and visualizing large genomic data sets, regardless of where data came from or where analysis took place. So even when using a separate command-line tool or other software program for analysis, SVS Core Plus can help eliminate many of the hassles of working with large data on the front-end and exploring it visually on the back-end.

Learn more about
Analytic Services »

Analytic Services

We have over a decade of collaborative experience working with the world's leading research organizations. With this, we offer a number of services to help accelerate your research.

Service Offerings

  • Genome-Wide SNP and CNV Association
  • Copy Number Detection
  • Genotype Calling
  • Imputation
  • Learn more...

 

CUSTOMER SUCCESS HIGHLIGHTS

03.07.12

Amplified Genes May Be Overexpressed, Unchanged, or Downregulated in Cervical Cancer Cell Lines

Vazquez-Mena, O et al.
Universidad Nacional Autónoma de México

02.07.12

Genetic Variation in Cell Death Genes and Risk of Non-Hodgkin Lymphoma

Schuetz, J et al.
University of British Columbia

12.21.11

Genome-Wide Association Study in Bipolar Patients Stratified by Co-Morbidity

Kerner, B & Lambert, C
UCLA & Golden Helix

11.10.11

A GWAS follow-up study reveals the association of IL12RB2 gene with Systemic Sclerosis in Caucasian populations

Bossini-Castillo, L. et al
Instituto de Parasitología y Biomedicina López-Neyra

09.30.11

Genetic Variants in TGF-β Pathway Are Associated with Ovarian Cancer Risk

Yin, J. et al
The University of Texas MD Anderson Cancer Center

06.10.11

Mutations in FYCO1 Cause Autosomal-Recessive Congenital Cataracts

Chen, J. et al
National Eye Institute

02.17.11

Risk HLA-DQA1 and PLA2R1 Alleles in Idiopathic Membranous Nephropathy

Stanescu, H. et al
University College London

01.30.11

Mutations in Fanconi anemia genes and the risk of esophageal cancer

 

Akbari, M. et al
University of Toronto

10.15.10

CoAIMs: A Cost-Effective Panel of Ancestry Informative Markers for Determining Continental Origins

Londin, E. et al
Coriell Institute for Medical Research

08.15.10

Common genetic variation in the HLA region is associated with late-onset sporadic Parkinson's disease

Hamza, T. et al
New York State Department of Health Wadsworth Center

07.11.10

Genome-wide association studies identify IL23R-IL12RB2 and IL10 as Behçet's disease susceptibility loci

Mizuki, N. et al
Yokohama City University Graduate School of Medicine, Japan

07.11.10

GWAS identifies variants in the MHC class I, IL10, & IL23R-IL12RB2 regions associated with Behçet's disease

Remmers, E. et al
National Institute of Arthritis and Musculoskeletal & Skin Diseases, USA

07.01.10

Genome-wide association study in alopecia areata implicates both innate and adaptive immunity

Petukhova, L. et al
Department of Dermatology,
Columbia University

06.26.10

Copy number variation and association over T-cell receptor genes—influence of DNA source

Schwienbacher, C. et al
Institute of Genetic Medicine, European Academy Bozen/Bolzano

04.28.10

Tourette syndrome is associated with recurrent exonic copy number variants

Sundaram, S. et al
Wayne State University

03.9.10

Assessment of variability in GWAS with CRLMM genotyping algorithm on WTCCC coronary artery disease

Zhang, L. et al
Center for Drug Evaluation & Research, FDA

03.03.10

Identification of Genome-wide Copy Number Variations and a Family-based Association Study of Avellino Corneal Dystrophy

Bae, J. et al
Sogang University, Shinsu-dong, Mapo-gu, Seoul, Republic of Korea

01.08.10

Genome-Wide Association Study Identifies ALDH7A1 as a Novel Susceptibility Gene for Osteoporosis

Guo, Y. et al
Xi'an Jiaotong University, Xi'an, People's Republic of China

05.07.09

Genome-wide Association Analysis Identifies PDE4D as an Asthma-Susceptibility Gene


Himes, B. et al
Brigham and Women's Hospital

UPDATES & INFO

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