DETECTION OF GENETIC ABNORMALITIES
The present invention provides assay systems and related methods for determining genetic abnormalities in mixed samples comprising cell free DNA from both normal and putative genetically atypical cells. Exemplary mixed samples for analysis using the assay systems of the invention include samples comprising both maternal and fetal cell free DNA and samples that contain DNA from normal cells and circulating cancerous cells.
1 . An assay system for providing a statistical likelihood of the presence or absence of a fetal aneuploidy comprising:
providing a maternal sample comprising maternal and fetal cell free DNA;
interrogating two or more polymorphic nucleic acid regions from a first chromosome;
detecting the interrogated polymorphic nucleic acid regions;
quantifying a relative frequency of alleles from the polymorphic nucleic acid regions from the first chromosome;
interrogating two or more selected nucleic acid regions from a second chromosome in the maternal sample;
detecting the interrogated two or more selected nucleic acid regions from the second chromosome;
quantifying a relative frequency of the interrogated two or more selected nucleic acid regions from the second chromosome;
comparing the relative frequency of the polymorphic nucleic acid regions from the first chromosome to the relative frequency of the polymorphic nucleic acid regions from the second chromosome;
calculating percent fetal cell free DNA in the maternal sample; and
providing a statistical likelihood of the presence or absence of a fetal aneuploidy using the calculated percent fetal cell free DNA in the maternal sample.
2 . The assay system of claim 1 , wherein at least the first chromosome is an autosome.
3 . The assay system of claim 2 , wherein both the first and second chromosomes are autosomes.
4 . The assay system of claim 1 , wherein calculating percent fetal cell free DNA comprises selecting polymorphic nucleic acid regions where maternal DNA is homozygous and fetal DNA is heterozygous.
5 . The assay system of claim 4 , wherein calculating percent fetal cell free DNA comprises computing a sum of low frequency alleles for the selected polymorphic nucleic acid regions.
6 . The assay system of claim 1 , wherein at least twenty-four polymorphic nucleic acid regions from the first chromosome and at least twenty-four polymorphic nucleic acid regions from the second chromosome are interrogated.
7 . The assay system of claim 6 , wherein at least forty-eight polymorphic nucleic acids from the first chromosome and at least forty-eight polymorphic nucleic acid regions from the second chromosome are interrogated.
8 . The assay system of claim 7 , wherein at least ninety-six polymorphic nucleic acids from the first chromosome and at least ninety-six polymorphic nucleic acid regions from the second chromosome are interrogated.
9 . The assay system of claim 1 , wherein an amplifying step is performed after one or both of the interrogating steps.
10 . The assay system of claim 1 , wherein an amplifying step is performed as part of one or both of the interrogating steps.
11 . The assay system of claim 9 , wherein the amplifying step is performed by PCR.
12 . The assay system of claim 10 , wherein the amplifying step is performed by PCR.
13 . The assay system of claim 1 , further comprising detecting levels of one or more non-maternally contributed region and quantifying a relative frequency of the one or more non-maternally contributed regions to determine the percent fetal cell free DNA in the maternal sample.
14 . An assay system for providing a statistical likelihood of the presence or absence of a fetal aneuploidy comprising:
providing a maternal sample comprising maternal and fetal cell free DNA;
interrogating two or more polymorphic nucleic acid regions from a first chromosome;
detecting the interrogated polymorphic nucleic acid regions;
quantifying a relative frequency of alleles from the first chromosome;
selecting quantified polymorphic nucleic acid regions to identify low frequency and high frequency alleles on the first chromosome;
interrogating two or more polymorphic nucleic acid regions from a second chromosome;
detecting the interrogated polymorphic nucleic acid regions;
quantifying a relative frequency of alleles from the second chromosome;
selecting quantified polymorphic nucleic acid regions to identify low frequency and high frequency alleles on the second chromosome;
calculating the percent fetal cell free DNA using the selected high frequency alleles and low frequency alleles;
providing a statistical likelihood of the presence or absence of a fetal aneuploidy using the calculated percent fetal cell free DNA in the maternal sample.
15 . The assay system of claim 14 , wherein at least the first chromosome is an autosome.
16 . The assay system of claim 15 , wherein both the first and second chromosomes are autosomes.
17 . The assay system of claim 14 , wherein at least twenty-four polymorphic nucleic acid regions from the first chromosome and at least twenty-four polymorphic nucleic acid regions from the second chromosome are interrogated.
18 . The assay system of claim 17 , wherein at least forty-eight polymorphic nucleic acids from the first chromosome and at least forty-eight polymorphic nucleic acid regions from the second chromosome are interrogated.
19 . The assay system of claim 18 , wherein at least ninety-six polymorphic nucleic acids from the first chromosome and at least ninety-six polymorphic nucleic acid regions from the second chromosome are interrogated.
20 . The assay system of claim 14 , wherein an amplifying step is performed after one or both of the interrogating steps.
21 . The assay system of claim 14 , wherein an amplifying step is performed as part of one or both of the interrogating steps.
22 . The assay system of claim 20 , wherein the amplifying step is performed by PCR.
23 . The assay system of claim 21 , wherein the amplifying step is performed by PCR.