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Related Concept Videos

Evolutionary Relationships through Genome Comparisons02:54

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Genome comparison is one of the excellent ways to interpret the evolutionary relationships between organisms. The basic principle of genome comparison is that if two species share a common feature, it is likely encoded by the DNA sequence conserved between both species. The advent of genome sequencing technologies in the late 20th century enabled scientists to understand the concept of conservation of domains between species and helped them to deduce evolutionary relationships across diverse...
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Small population sizes put a species at extreme risk of extinction due to a lack of variation, and a consequent decrease in adaptability. This weakens the chances of survival under pressures such as climate change, competition from other species, or new diseases. Large populations are more likely to survive pressures such as these, as such populations are more likely to harbor individuals that have genetic variants that are adaptive under new stresses. Small populations are much less...
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A population is composed of members of the same species that simultaneously live and interact in the same area. When individuals in a population breed, they pass down their genes to their offspring. Many of these genes are polymorphic, meaning that they occur in multiple variants. Such variations of a gene are referred to as alleles. The collective set of all the alleles within a population is known as the gene pool.
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Genetic variation is the diversity in DNA sequences found among individuals of the same species. This diversity is crucial for a species' survival because it helps organisms adapt to environmental changes. Genetic variation begins with fertilization, where an egg and sperm cell merge. Each of these cells carries 23 chromosomes, up to 46 in the fertilized egg. Chromosomes are long DNA strands that contain genes, the basic units of heredity.
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Combined Immunofluorescence and DNA FISH on 3D-preserved Interphase Nuclei to Study Changes in 3D Nuclear Organization
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Fine-Scale Genetic Structure in Finland.

Sini Kerminen1, Aki S Havulinna1,2, Garrett Hellenthal3

  • 1Institute for Molecular Medicine Finland, University of Helsinki, 00014, Finland.

G3 (Bethesda, Md.)
|October 7, 2017
PubMed
Summary
This summary is machine-generated.

This study reveals Finland

Keywords:
haplotype sharingpopulation geneticspopulation structure

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Area of Science:

  • Population genetics
  • Computational genomics
  • Human ancestry

Background:

  • Geographically precise reference datasets are crucial for accurate individual-level ancestry estimation.
  • Finland's unique population structure, predating the 1950s, offers a valuable case study.

Purpose of the Study:

  • To analyze the genetic structure of the Finnish population using a precisely defined reference dataset.
  • To investigate the relationship between genetic clusters, historical settlement, and linguistic regions in Finland.

Main Methods:

  • Utilized dense genotype data from 2376 individuals in the 1997 FINRISK Study.
  • Applied haplotype-based computational methods: ChromoPainter (CP) and FineSTRUCTURE (FS).

Main Results:

  • Revealed a highly geographically clustered genetic structure within Finland.
  • Identified a main genetic division strongly correlating with the 1323 Nöteborg treaty border.
  • Observed significant regional genetic substructure, unlike the more homogeneous UK population.

Conclusions:

  • Finnish population genetics reflect historical settlement and linguistic patterns.
  • CP + FS methods, with extensions, are effective for detailed population structure analysis.
  • Future availability of similar reference datasets will advance forensic genetics and association studies.