Methods for copy number determination
View Patent ↗The invention generally relates to a method for determining carrier or disease status with respect to a particular disease or condition. In certain embodiments, methods of the invention involve obtaining a sample including nucleic acid from a subject. The nucleic acid includes a genomic locus that is diagnostic for an autosomal recessive disease. The nucleic acid is captured and isolated from the sample and further sequenced. The method further includes analyzing sequence reads to determine a copy number of the captured nucleic acid and further determine a disease status based upon the copy number.
1. A method for determining carrier status of spinal muscular atrophy, the method comprising the steps of:
capturing, using non-naturally occurring synthesized molecular inversion probes, nucleic acid corresponding to a first genomic locus and second genomic locus on intron 7 of an SMN1 or SMN2 gene;
sequencing, using a sequencing instrument, said captured nucleic acids;
measuring copy number of said captured nucleic acids; and
determining carrier status based upon the copy number.
2. The method of claim 1 , wherein said first and second genomic loci are rs212214 and rs212213.
3. The method of claim 1 , wherein said sequencing step comprises a Sanger sequencing method or a next-generation sequencing method.
4. The method of claim 1 , wherein said capturing step comprises isolating said nucleic acid from a sample comprising nucleic acid from a subject.
5. The method of claim 4 , wherein said sample is a maternal blood sample.
6. The method of claim 5 , wherein said maternal blood sample comprises cell free circulating nucleic acid.
7. The method of claim 6 , wherein at least a portion of the cell free circulating nucleic acid is from a fetus being carried within the subject.
8. A method of determining carrier status of spinal muscular atrophy, the method comprising the steps of:
obtaining a sample from a patient comprising nucleic acid;
measuring for a copy number variant at two intron 7 genomic loci of said nucleic acid, wherein said intron 7 genomic loci are in an SMN1 gene or SMN2 gene, and wherein the measuring step comprises:
introducing molecular inversion probes to said sample that hybridize to and capture said intron 7 genomic loci; and
sequencing said captured intron 7 genomic loci; and
determining carrier status of said individual based on the copy number variant in said intron 7 genomic loci.
9. The method of claim 1 , wherein the step of capturing copy number of said captured nucleic acids comprises not capturing or sequencing nucleic acids in exon 7 or exon 8 of the SMN1 or SMN2 gene.
10. The method of claim 8 , wherein the step of capturing copy number of said captured nucleic acids comprises not capturing or sequencing nucleic acids in exon 7 or exon 8 of the SMN1 or SMN2 gene.