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      <image:title>Blog - How To Read Your Paternity Test Results - Make it stand out</image:title>
      <image:caption>Whatever it is, the way you tell your story online can make all the difference.</image:caption>
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      <image:loc>https://images.squarespace-cdn.com/content/v1/62165c513952312109c0ea08/cb235b06-4750-4781-9925-285f5a8a9c70/D63_0068-1L+labeled.jpg</image:loc>
      <image:title>Blog - How To Read Your Paternity Test Results - Paternity Test Results Overview</image:title>
      <image:caption>Your paternity test results contains the following sections, each containing important information. Identifying Information Marker/Allele Size Data Table Statistics Conclusion Verification(s)</image:caption>
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      <image:title>Blog - How To Read Your Paternity Test Results</image:title>
      <image:caption>Our processing laboratory tests at least 24 different locations on each testing parties' DNA, known as "Markers", and compare both. A child's DNA consists of one copy of the DNA segment from the mother, and one copy from the father, giving us what are called "alleles". The way these are compared is by using specific technology to determine the length of each parties' alleles, and comparing the lengths at each location to determine the number of matches. In the example below, the child shown (labeled under the CL column) has two sets of alleles tested at each marker, and in most cases, at least one of these matches with the alleged father's (labeled under the AFL column) alleles. There are also cases where there was a mutation in either the child’s or the alleged father’s genetic makeup at that marker. Our analysts take mutations into account when doing their calculations and reaching conclusions, so even if there is a mismatch, the man might still be considered the biological father of the child tested.</image:caption>
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      <image:title>Blog - Invasive vs. Non-Invasive Prenatal Paternity Testing - For Amniocentesis, a healthcare provider starts by inserting a needle into the mother’s abdomen to draw out a small sample of amniotic fluid. The potential father has a buccal (cheek) swab done to collect a DNA sample. The lab then compares DNA from the sample to the mother’s and potential father’s DNA.</image:title>
      <image:caption>Amniocentesis takes place between the 15th and 20th weeks of pregnancy.</image:caption>
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      <image:loc>https://images.squarespace-cdn.com/content/v1/62165c513952312109c0ea08/eaed7a03-fec6-4a52-96bd-237e7de83171/Chorionic+Villus+Sampling+%28CVS%29+Diagram.png</image:loc>
      <image:title>Blog - Invasive vs. Non-Invasive Prenatal Paternity Testing - For Chorionic Villus Sampling, a healthcare provider starts by inserting a catheter through the mother’s cervix. A small sample of fetal DNA is then collected from the placenta. The potential father has a buccal (cheek) swab done to collect a DNA sample. The lab then compares DNA from the sample to the mother’s and potential father’s DNA.</image:title>
      <image:caption>Chorionic Villus Sampling typically takes place between 10 to 13 weeks after a woman’s last menstrual period.</image:caption>
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