Difference between revisions of "The second Korean human genome"

From Kogic.net
 
Line 6: Line 6:
 
==== See also ====
 
==== See also ====
  
<span style="font-size:16px;">[http://kogic.net/The_first_Korean_genome_sequence_and_analysis:_Full_genome_sequencing_for_a_socio-ethnic_group T]</span>[http://kogic.net/The_first_Korean_genome_sequence_and_analysis:_Full_genome_sequencing_for_a_socio-ethnic_group <span style="font-size:16px;">he first Korean human genome</span>]<br/> [[A_korean_genome_sequence_is_announced_to_the_public_using_a_Solexa_sequencer_2008_12_04|<span style="font-size:16px;">A korean genome sequence is announced to the public using a Solexa sequencer 2008 12 04</span>]]<br/> <br/> &nbsp;
+
[http://kogic.net/The_first_Korean_genome_sequence_and_analysis:_Full_genome_sequencing_for_a_socio-ethnic_group <span style="font-size:16px;">The&nbsp;</span>]<span style="font-size:16px;">[http://kogic.net/The_first_Korean_genome_sequence_and_analysis:_Full_genome_sequencing_for_a_socio-ethnic_group first Korean human genome]</span><br/> [[A_korean_genome_sequence_is_announced_to_the_public_using_a_Solexa_sequencer_2008_12_04|<span style="font-size:16px;">A korean genome sequence is announced to the public using a Solexa sequencer 2008 12 04</span>]]<br/> <br/> &nbsp;

Latest revision as of 12:39, 24 June 2020

A highly annotated whole-genome sequence of a Korean individual



Recent advances in sequencing technologies have initiated an era of personal genome sequences. To date, human genome sequences have been reported for individuals with ancestry in three distinct geographical regions: a Yoruba African, two individuals of northwest European origin, and a person from China1,2,3,4. Here we provide a highly annotated, whole-genome sequence for a Korean individual, known as AK1. The genome of AK1 was determined by an exacting, combined approach that included whole-genome shotgun sequencing (27.8 coverage), targeted bacterial artificial chromosome sequencing, and high-resolution comparative genomic hybridization using custom microarrays featuring more than 24 million probes. Alignment to the NCBI reference, a composite of several ethnic clades5,6, disclosed nearly 3.45 million single nucleotide polymorphisms (SNPs), including 10,162 non-synonymous SNPs, and 170,202 deletion or insertion polymorphisms (indels). SNP and indel densities were strongly correlated genome-wide. Applying very conservative criteria yielded highly reliable copy number variants for clinical considerations. Potential medical phenotypes were annotated for non-synonymous SNPs, coding domain indels, and structural variants. The integration of several human whole-genome sequences derived from several ethnic groups will assist in understanding genetic ancestry, migration patterns and population bottlenecks.

Link to full article

Nature. 2009.07.08

 

See also

The first Korean human genome
A korean genome sequence is announced to the public using a Solexa sequencer 2008 12 04