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  Getting Started with Borland Genetics: A Step-by-Step Guide Borland Genetics is a DNA database that integrates an extensive suite of tools to help you reconstruct the DNA of your ancestors. It’s designed for genealogists who want to go beyond just discovering cousin matches and into the realm of reconstructing family members’ genetic profiles. Whether you're just starting out in genetic genealogy or looking to dive deeper into DNA reconstruction, this guide will walk you through the key steps to get up and running with Borland Genetics. 1. Who Uses Borland Genetics? The users who benefit the most from the tools at Borland Genetics are those who have tested multiple family members.  The original idea that led to the development of Borland Genetics was that the product would be helpful when, for example, DNA tests were provided to attendees at a family reunion, the tools would automate the process of analyzing the shared DNA among the testers to reconstruct the genome of their shar

Explore Advanced Chromosome Mapping Tools with Borland Genetics

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At Borland Genetics, we offer a suite of cutting-edge tools designed to take your genetic genealogy research to the next level. Whether you're reconstructing ancestor DNA or visually exploring chromosome inheritance, our tools give you the power to dive deep into your DNA connections. Here's a look at our most powerful chromosome mapping features: 1. HIR Mapper The HIR Mapper is a dynamic tool that generates chromosome maps by identifying segments of DNA shared between your focus donor and matches in the Borland Genetics database. The resulting phase map visualizes recombination points from the most recent generation of inheritance, helping you track which segments came from which parent. Key Features : Incorporates matches from Borland Genetics and GEDmatch Segment Search. Displays DNA matches, grouped by segment or block, with options to review and adjust. Outputs phase maps to help visualize inherited DNA and recombination points. Perfect for users mapping DNA inherited fr

Reconstructing My Great-Grandparents (As The Creeper Tour Rolls On)

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Kevin and Rolf exhibiting Borland Genetics in Sweden As many readers may be aware, Borland Genetics has been promoting uploads to the site throughout 2022 via a hybrid in-person/virtual string of appearances at industry tradeshows, genealogy society events, genealogy vlogs, etc., all under the penumbra of the "2022 Creeper Tour."  So far, the tour has passed through Baltimore, Cincinnati, Sacramento, Ottawa, Indianapolis, Portland (Oregon),  Skövde (Sweden), and Burbank, and upcoming dates are scheduled for Minneapolis (virtual), Sydney (Australia), Salt Lake City, Richmond, Sandusky, Milwaukee, and finally back to Baltimore (as the Tour extends through 2023). Some of the dates thus far  have been expo hall exhibits with opportunity to meet me in-person and discuss Borland Genetics reconstruction techniques, while others took the form of virtual talks where I presented topics including DNA inheritance, DNA reconstruction, interpreting one's DNA results, the future of DNA

Introducing the Borland Genetics Segment Lab

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  It occurred to me today that I have not yet done a tutorial on how to use the Borland Genetics “Segment Lab” tool.   Introduced as part of last October’s anniversary “Fall Features Release,” it’s one of the newest tools on the site, and probably also one of the most under-utilized.   Hopefully, this demonstration will show how it’s also one of the most valuable tools on the site. The Segment Lab is Borland Genetics’ native chromosome map/phase map editor.   While a far cry from a robust chromosome mapping solution like DNAPainter, it has specialized features that I designed to make our task of ancestor DNA reconstruction easier, and to help maximize the reconstruction coverage of our output ancestor kits. Before we dive into using the tool, I want to point out that the Segment Lab is NOT a tool that creates a phase map from scratch.   At Borland Genetics, that’s what the HIR Mapper does, and when it comes to mapping matches from outside the Borland Genetics platform, DNAPainter i
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Help!   My Segments Are So Sticky! Back in the day, it used to be popular to refer to certain segments as “sticky” when they appeared to be passed down from generation to generation untouched.   That sort of name-calling has reduced greatly now that we have a clearer understanding of the statistical rules that our chromosomes follow as a result of random recombination.   It turns out that the smaller a segment, the more likely it is to escape the chopping block of recombination in each generation and instead either be passed to the child in full or not at all.   Let’s take a look at some numbers and see how this plays out. As our starting point, we’re going to go back to our definition of centiMorgan, as explained in my blog from a few weeks ago about the statistical impossibility of two full siblings not sharing any DNA segments.   If you missed that one, that’s OK, here’s the way I like to think about a cM:   A cM is a unit that denotes a span of a chromosome that has