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Like sports, geopolitics, history. Living in Tampere, Finland. Y-DNA: N-M232. Trying to find missing parts of my family tree :)":1,"#¿Veré otra diferencia en mis resultados con la nueva prueba?":1,"#Las muestras antes del 2 de marzo de 2026 se analizan con el genotipado de microarrays real. Todas las noticias prueba de Family Finder personas contras requeday de esa se fechaán con el nuevo panel de secuenciación.":1,"#Daniella Mella":1,"#Esta cookie se conoce como Google Cloud Load Balancer, establecida por el proveedor Google. Se utiliza para el balanceo de carga HTTPS externo de la infraestructura en la nube con Google.":1,"#Are you sure you want to mark test taker Susana Cabral as deceased? This cannot be undone.":1,"#We just sent a verification code to your email nl***ac@gmail.com. Please enter the 6-digit verification code.":1,"#Vogel, Marcelo":1,"#Roopkund 40":1,"#IN150097T101339":1,"#The price of the Family Finder test will remain the same.":1,"#What will the new Family Finder test cost?":1,"#The new panel will focus coverage on about 280 million base pairs of the human genome, which will include the approximately 700,000 SNPs previously reported from the GSA microarray chip.":1,"#Targeted next-generation sequencing aims to read selected portions of the human genome at high coverage rather than the complete human genome.":1,"#What does the new Family Finder test do?":1,"#Family Finder has transitioned to a next-generation sequencing panel. All samples that begin processing on or after March 2, 2026, will be tested using this new panel. Your existing results will re...":1,"#Family Finder has transitioned to a next-generation sequencing panel. All samples that begin processing on or after March 2, 2026, will...":1,"#This change allows us to deliver more precise autosomal results today while creating a strong foundation for future reports and tools.":1,"#Twist Family Finder FAQ – Help | FamilyTreeDNA":1,"#Over time, we expect multiple sequencing approaches to coexist, giving customers the ability to choose the tools that best support their research goals.":1,"#For autosomal genetic genealogy, we believe our new targeted sequencing panel represents our new gold standard. It was designed specifically to deliver consistent, high-coverage data across the regions that matter most for matching, relationship inference, and future genealogical analysis, while remaining accessible and affordable for long-term research.":1,"#Different sequencing approaches provide different views of your DNA, much like comparing an aerial photo of your home to a view from your front yard. Each approach offers strengths depending on the type of insight you are seeking.":1,"#That depends on what you are trying to learn.":1,"#There are different sequencing approaches that replace microarrays. Which one is best?":1,"#We are also excited about the potential for new insights from high coverage data and will continue evaluating these possibilities as our database of panel-based autosomal tests grows.":1,"#This consistency is especially important for analyses such as Y-DNA and planned mtDNA haplogroup estimations within the Family Finder product.":1,"#The targeted enrichment panel provides more consistent, higher-quality reporting across the regions of the genome that we have determined are most useful for genetic genealogy.":1,"#Why didn’t FamilyTreeDNA use low coverage Whole Genome Sequencing?":1,"#Starting March 2, 2026, the Family Finder test will be performed using next-generation sequencing using a custom targeted enrichment panel. This new approach consistently reports a higher percentage of the genetic information most relevant to genealogy, with improved accuracy and consistency.":1,"#This approach focuses on sequencing power where it matters most for family history research.":1,"#Applying high coverage to a carefully selected portion of the genome allows us to deliver greater precision for genetic genealogy at a much more affordable price point than high coverage Whole Genome Sequencing.":1,"#Why did FamilyTreeDNA choose a targeted sequencing panel instead of high coverage Whole Genome Sequencing?":1,"#Family Finder tests run on the new sequencing panel use the same stored DNA sample and do not require more DNA than the previous microarray genotyping test.":1,"#Does the new Family Finder test require more DNA than the current test?":1,"#Additional data formats may become available later in 2026.":1,"#The same autosomal data downloads available today will be available immediately for tests processed on the new panel. For compatibility, autosomal downloads will continue to be provided in hg37 format.":1,"#Yes. You will still be able to download your data.":1,"#Will I be able to download my data, and will the format change?":1,"#We will share clear details about timing, eligibility, and pricing before this upgrade becomes available.":1,"#FamilyTreeDNA’s Family Finder test currently uses a custom Global Screening Array (GSA) microarray chip that reports about 700,000 SNPs across the human genome.":1,"#Yes. Once we begin using results from the new panel for new features, we plan to offer existing Family Finder customers an optional upgrade to the new panel at a discounted price.":1,"#Will there be an upgrade option for existing Family Finder customers?":1,"#Existing Family Finder results will remain exactly as they are and will continue to work as expected.":1,"#I already took a Family Finder test. Will my existing test automatically be reprocessed on the new panel?":1,"#Our first priority is to ensure that customers receive the same trusted experience they expect today, including matching and ethnicity results. Once we have built a strong foundation of data from the new panel, we will begin introducing new reports and tools over time.":1,"#Not initially.":1,"#Will I see a difference in my results from the new test?":1,"#Samples received before March 2, 2026 will be run using the current microarray genotyping. All new Family Finder tests received after that date will be processed using the new sequencing panel.":1,"#If I buy a Family Finder test now, will it be processed with the new panel or the current one?":1,"#What’s changing?":1,"#Family Finder has transitioned to a next-generation sequencing panel. All samples that begin processing on or after March 2, 2026, will be tested using this new panel. Your existing results will remain valid, and matching and ethnicity will continue to work just as they do today. New testers do not need to wait. Existing testers will have the option to upgrade later at a discounted price. No action is needed right now.":1,"#Luis pena":1,"#Monday, February 23, 2026 at 5:55pm":1,"#Monday, February 23, 2026 at 3:41pm":1,"#Francisco, yes the difference in the Private Variants (and total variants between your lone Spanish subclade of BY78943 compared to the English and German branches parallel yours is because your line is under-sampled. What we have found is that the more men test, the more SNPs/Variants are discovered. This is because a weak read on a variant in one man's test can be verified by a stronger read in another man's test on the same branch. And so, the more the testers the more SNPs are discovered. View the locations the GlobeTrekker gives for any individual Haplogroup with a skeptical eye. No one truly knows the exact location most early SNP arose. And GlobeTrekker does not use Archelogical finds below DF27. Rather, the \"path\" for any given SNP is determined by Averaging the Self-Reported Location for the Most Distant Known Ancestor (usually from the 1700s t0 1800s) of all the men under that Haplogroup. Since your haplogroup is dominated by English and German testers, that pulls the location of BY78943 much farther north than it probably was in 1350 BC. For all we know, BY78943 arose close Spain, but the German and English branches moved north leaving their Spanish kinsmen behind. From the data we have we just can't know where the first man positive for BY78943 lived. Also recognize that DF27 originated somewhere in southern to southcentral France, or perhaps in Spain. And the Hallstatt and LaTene Culture finds did not evidence Haplogroups leading to DF27. Hallstatt was dominantly G-L497 and R-U106 along with a few other Neolithic Haplogroups. yDNA finds in the LaTene Cultures likewise are reported as R-M269 >> L21 >> M222, I-M253 and E-M215. [U106 AND L21 both branched away from our ancestors about 3050 BC 300 years before DF27 arose.] In fact, DF27 existed in Spain in great numbers 600+ years before Hallstatt Culture arose and 1300+ years. before LaTene Culture first sprouted. Indeed, even L21, which is found associated with LaTene had arrived on an Island off the northern coast of Ireland 800 years before Hallstatt and 1500 years before LaTene. So, we are pre-Celtic. Some linguists theorize that the Celtic Language arose on the Atlantic coast as a trade language where by 1500 BC we left individual remains along the coast of Britain, likely as traders. [Note, there is no evidence that the Celtic Language and Haltstatt/LaTene Material Culture became dominant in Britain and Ireland before about 900 BC.] In the meantime our DF27 ancestors were plying the seas (both Atlantic and Mediterranean) and possibly roaming the land as far a Germany as traders between 2000 and 1500 BC, long before Hallstatt began. More importantly for you, you have a y67 GD=7 match. If he upgraded to Big Y you would undoubtedly create a new Branch below BY78943 and discover more SNPs, blazing the trail for others on your branch.":1,"#I'm investigating my assignment to R-BY78943 (Rodriguez; Almeria, Spain). Interestingly, the English branch under the same node shows nearly double the SNPs. Given the (Globetrekker) MRCA of 800 BC in Northern France, I suspect an Iron Age Celtic (Gaulish) origin. The sequence would be: Hallstatt > (La Tène) > Celtiberians > Castillians/Aragoneses > repopulation of Almería during The Reconquista. Additionally, I have a 7-step match at the Y-67 level (MRCA ~1100 CE per FTDNATiP) whose paternal lineage reportedly originates from the Canary Islands. This connection leads me to wonder if this branch was later dispersed via the Norman expedition of Jean de Béthencourt in 1402 and is related to the Norman contribution to the Iberian Reconquista. This would link the Northern French origin with the Canarian presence. Is it common to see such a considerable branch length discrepancy within R-BY78943, or could this suggest that the Spanish line is currently under-sampled in the tree?":1,"#We just sent a verification code to your email lu***ti@hotmail.com. Please enter the 6-digit verification code.":1,"#Paseo Aragón 30 22540 Altorricón (Huesca)":1,"#Paseo Aragón 39 22540 Altorricón (Huesca)":1,"#Paseo Aragón 31 22540 Altorricón (Huesca)":1,"#Paseo Aragón 3 22540 Altorricón (Huesca)":1,"#Paseo Arriba 12 08024 Barcelona (Barcelona)":1,"#Paseo Arriba 33 08024 Barcelona (Barcelona)":1,"#Paseo de los Fueros de Aragón 32 50178 La Almolda (Zaragoza)":1,"#Paseo de Aragón 32 50172 Alfajarín (Zaragoza)":1,"#Paseo de Ramiro I de Aragón 4 SO 32 50196 La Muela (Zaragoza)":1,"#Paseo de los Adarves 32 19300 Molina de Aragón (Guadalajara)":1,"#Paseo Arriba 16 08024 Barcelona (Barcelona)":1,"#Paseo Cortes de Aragón 32 50300 Calatayud (Zaragoza)":1,"#Paseo de las Cortes de Aragón 4 SO 32 50300 Calatayud (Zaragoza)":1,"#Paseo de las Cortes de Aragón 8 SO 32 50300 Calatayud (Zaragoza)":1,"#Paseo de los Fueros de Aragón 1 BJ 32 50500 Tarazona (Zaragoza)":1,"#Paseo de los Fueros de Aragón 1 SO 32 50500 Tarazona (Zaragoza)":1,"#Paseo de los Fueros de Aragón 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