ARIMA GENOMICS, INC. — Department of Health and Human Services SBIR Phase I: NIAID

ARIMA GENOMICS, INC. — SBIR Phase I award from Department of Health and Human Services.

Amount
$274,115
Agency
Department of Health and Human Services · National Institutes of Health
Program / Phase
SBIR · Phase I
Topic
NIAID
Solicitation
PA16-414
NAICS
Place of performance
CA
Period
2016-07-12 → 2017-06-30

Description

Maximal resolution and full length phasing for next generation MHC typing Arima Genomics Project Summary Abstract The Major Histocompatibility complex MHC locus is among the most polymorphic loci in the genome and harbors genes that play critical roles in human immune health and disease The polymorphic nature of the MHC locus allows for encoding every individual with a unique immune cell profile hence matching HLA genes among donors and recipients has been a critical step in mitigating immune rejections following organ transplants Advances in next generation sequencing technologies have increased the popularity of DNA sequencing as a means of typing the HLA locus for its clinical relevance Yet current HLA typing technologies ignore potentially important DNA variants type gene by gene at low resolution and fail to haplotype phase non HLA genes and other non coding alleles in the MHC locus that are necessary for optimal donor recipient matching Arima Genomics has recently developed an innovative new approach to generate full length haplotypes of the MHC locus at high resolution building on our proprietary HaploSeq technology for constructing chromosome spanning haplotypes in the human genome Our new technology andquot HaploSeq Mxandquot is capable of phasing the entire Mb HLA locus onto a single haplotype block at resolution and accuracy with just x sequencing depth As a cost effective next generation haplotyping technology HaploSeq Mx is poised to underpin a new standard in high resolution locus spanning MHC typing The objectives of Arima Genomicsandapos proposed Randamp D efforts involve improving HaploSeq Mxandapos s targeting efficiency to further reduce sequencing costs and advance the method to clinical utility developing computational approaches to improve the accuracy of HaploSeq Mx even further to andgt and demonstrating feasibility of HaploSeq Mx for MHC typing patient samples in a hematopoietic stem cell transplantation HSCT study with clinical collaborators at the Immunogenetics and Transplantation Laboratory ITL at the UCSD Center for Advanced Laboratory Medicine CALM while developing a new algorithm for donor recipient matching Successful completion of our research aims will contribute invaluable new knowledge to ongoing investigations of how human genetic variation influences patient outcomes in transplants and will substantially advance the capabilities of our HLA typing technology toward commercial viability in clinical applications HaploSeq Mx promises to greatly enhance our understanding of human genetics in health and contribute to the realization of personalized medicine Maximal resolution and full length phasing for next generation MHC typing Arima Genomics Project Narrative Determining the haplotype of the MHC locus or MHC typing is a critical step in identifying potential matches between donors and recipients for allogeneic transplants but current methods evaluate only HLA genes missing information from hundreds of other genes as well as non coding elements in this locus Consequently this can lead to potential adverse outcomes due to suboptimal MHC matching Arima Genomics recently extended our innovative HaploSeq technology as a novel cost effective approach to accurately haplotype the entire human MHC locus at high resolution to phase HLA genes non HLA genes and non coding elements in a single haplotype This new HaploSeq Mx method will enable high fidelity matching of donor and recipient for hematopoietic stem cell transplants and other allograft procedures and will contribute to a greater understanding of the human genomeandapos s role in transplant outcomes