Genetic Alliance adds three labs to global genomics network

Jul. 24, 2026
By AI, Created 13:00 UTC, Jul 24, 2026, AGP -

Genetic Alliance has added Children’s Mercy, SN Genelab and Xcelom to its global laboratory network, expanding no-cost whole genome sequencing for eligible families in 14 countries. The move increases access to rare-disease testing in the U.S., India and Hong Kong as the program passes nearly 4,000 underserved families served.

Why it matters: - Genetic Alliance is expanding access to clinical whole genome sequencing for children and families with suspected genetic conditions. - The new lab partners add capacity in the U.S., India and Hong Kong, extending the network into more regions. - The program has already delivered no-cost genomic testing to nearly 4,000 underserved families.

What happened: - Genetic Alliance announced that Children’s Mercy in Kansas City, Missouri; SN Genelab in Surat, India; and Xcelom in Hong Kong have joined its global genomics network. - The three laboratories will provide clinical whole genome sequencing using Pacific Biosciences HiFi long-read technology at no cost to eligible families. - Families are referred through Genetic Alliance’s network of 26 clinical sites across 14 countries. - The announcement came July 24, 2026.

The details: - The three laboratories were selected through a competitive application process. - Selection was based on clinical genomic testing quality, robust quality systems and a commitment to equitable access to genomic medicine. - Each laboratory met Genetic Alliance’s standards for clinical quality, technical capability and collaborative engagement. - Children’s Mercy brings pediatric genomic medicine and rare-disease diagnosis expertise to the network. - SN Genelab is Genetic Alliance’s first laboratory partner in India. - Xcelom is Genetic Alliance’s first laboratory partner in Hong Kong. - Xcelom, a subsidiary of Berry Genomics, operates a CAP-accredited facility and offers clinically validated long-read whole genome sequencing and long-read targeted assays. - SN Genelab says it has performed more than 1.5 million genetic tests and offers more than 650 genomic diagnostic tests. - SN Genelab’s platform includes PacBio Revio and Oxford Nanopore long-read sequencing, Illumina NovaSeq X and NovaSeq 6000 systems, microarray platforms, AI-ML enabled karyotyping and in-house bioinformatics. - Genetic Alliance says the added labs will help more children with suspected rare genetic diseases receive testing regardless of where they live.

Between the lines: - The network is leaning on geographically distributed labs to reduce access gaps in rare-disease diagnosis. - Adding first-ever partners in India and Hong Kong suggests Genetic Alliance is pushing deeper into Asia-Pacific and South Asia. - The focus on long-read sequencing points to a strategy built around harder-to-detect genetic changes that can matter in rare disease workups. - Ryan Taft, Genetic Alliance’s chief scientific officer, said each added laboratory brings new expertise, technologies and opportunities for children who might otherwise never receive a genetic diagnosis.

What’s next: - Genetic Alliance will continue using its international network of clinical sites, laboratories, researchers and community organizations to expand equitable access to genomic testing. - The organization is also seeking donations to support the network through a linked fundraising page. - As the network grows, more referred families could gain access to no-cost testing and downstream care, support and research connections.

The bottom line: - Genetic Alliance is scaling a global rare-disease testing network by adding three more laboratories and widening access to long-read genomic sequencing for underserved families.

Disclaimer: This article was produced by AGP Wire with the assistance of artificial intelligence based on original source content and has been refined to improve clarity, structure, and readability. This content is provided on an “as is” basis. While care has been taken in its preparation, it may contain inaccuracies or omissions, and readers should consult the original source and independently verify key information where appropriate. This content is for informational purposes only and does not constitute legal, financial, investment, or other professional advice.

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