Methods and compositions for screening and treating developmental disorders
This document provides methods and materials related to genetic variations of developmental disorders. For example, this document provides methods for using such genetic variations to assess susceptibility of developing Autism Spectrum Disorder.
1. A method of hybridizing a nucleic acid probe or synthesizing a nucleic acid product comprising:
(a) hybridizing a nucleic acid probe to a polynucleic acid by nucleic acid hybridization or microarray analysis, or synthesizing a nucleic acid product from a polynucleic acid by PCR or sequencing, wherein the polynucleic acid is from a sample from a human subject that has Autism Spectrum Disorder (ASD); and
(b) detecting a genetic variation in (i) the polynucleic acid by nucleic acid hybridization or microarray analysis or (ii) the nucleic acid product by PCR or sequencing, wherein the genetic variation is a copy number variant (CNV), wherein the CNV is within a TBCK gene, wherein the CNV comprises SEQ ID NO: 420 or the full length complement thereof.
2. The method of claim 1 , wherein the CNV is a loss of a sequence comprising SEQ ID NO: 420 or the full length complement thereof.
3. The method of claim 2 , wherein the CNV is a loss of a sequence consisting of SEQ ID NO: 420 or the full length complement thereof.
4. The method of claim 1 , wherein the nucleic acid product synthesized from the polynucleic acid comprises cDNA.
5. The method of claim 1 , wherein the polynucleic acid comprises a nucleic acid from blood, saliva, urine, serum, tears, skin, tissue, or hair from the subject.
6. The method of claim 1 , wherein the method comprises isolating polynucleotides; and performing a microarray analysis of the polynucleotides.
7. The method of claim 6 , wherein the microarray analysis comprises Comparative Genomic Hybridization (CGH) array analysis.
8. The method of claim 1 , wherein the microarray analysis is selected from the group consisting of a Comparative Genomic Hybridization (CGH) array analysis and an SNP array analysis.
9. The method of claim 1 , wherein the sequencing comprises high throughput sequencing.
10. The method of claim 1 , wherein the whole genome of the subject is analyzed.
11. The method of claim 1 , wherein the whole exome of the subject is analyzed.
12. The method of claim 1 , wherein the detecting comprises detecting a first genetic variation that is the CNV with a sequence of SEQ ID NO: 420 or the full length complement thereof, wherein the first genetic variation and a second genetic variation are in a panel comprising two or more genetic variations.
13. The method of claim 12 , wherein the panel comprises 50 or more genetic variations.
14. The method of claim 12 , wherein the panel comprises 100 or more genetic variations.
15. The method of claim 1 , wherein the detecting comprises detecting two or more genetic variations.
16. The method of claim 1 , wherein the microarray analysis comprises an in-silico analysis.
17. A method of treatment comprising administering an agent having a therapeutic benefit for treatment of ASD, to a subject in need thereof, wherein the subject has been identified as having the genetic variation according to the method of claim 1 .