Evidence map›Paper›PMID 21169219›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2011

Completely phased genome sequencing through chromosome sorting.

Hong Yang, Xi Chen, Wing Hung Wong

Erratum issuedAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 57 papers.

0numbers the graph read from it
0cells of the map it votes in
57citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

57 citing papers in PubMed.

  1. Current Progress in Phased Genome Assembly from Long-Read DNA Sequencing Data.Methods in molecular biology (Clifton, N.J.) · 2025
    Review
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  12. Homologue-specific chromosome sequencing characterizes translocation junctions and permits allelic assignment.DNA research : an international journal for rapid publication of reports on genes and genomes · 2018
    Article
  13. Article
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  15. Article
  16. Review
  17. Recent Advances in Experimental Whole Genome Haplotyping Methods.International journal of molecular sciences · 2017
    Review
  18. Article
  19. Article
  20. Article
4 · The record

Corrections and comments

  • Erratum issued
5 · Who and what money

Authors and funding

3 authors.

Hong YangDepartment of Statistics, Stanford University, Stanford, CA 94305-4065, USA.
Xi Chen
Wing Hung Wong

Funding

Cis-analysis of expression and ChIP data on Shh pathwayR01HG003903 · NHGRI · STANFORD UNIVERSITY · PI WONG, WING H. · 2006 to 2010
$2.5M
Statistical Analysis of Exon ArraysR01HG004634 · NHGRI · STANFORD UNIVERSITY · PI WONG, WING H. · 2008 to 2011
$1.4M
Statistical and computational analysis in whole genome sequencing studies.R01HG007834 · NHGRI · STANFORD UNIVERSITY · PI WONG, WING H. · 2014 to 2016
$892k
NHGRI NIH HHS R01 HG003903NHGRI NIH HHS R01HG003903NHGRI NIH HHS R01 HG004634NHGRI NIH HHS R01HG004634NHGRI NIH HHS R01 HG007834
6 · The paper itself

Abstract

The two haploid genome sequences that a person inherits from the two parents represent the most fundamentally useful type of genetic information for the study of heritable diseases and the development of personalized medicine. Because of the difficulty in obtaining long-range phase information, current sequencing methods are unable to provide this information. Here, we introduce and show feasibility of a scalable approach capable of generating genomic sequences completely phased across the entire chromosome.

Indexed as

Chromosomes, HumanDNA PrimersFlow CytometryGenome, HumanGenotypeHaplotypesHumansMutationPolymorphism, Single NucleotideSequence Analysis, DNADNA Primers

Identifiers

PMID21169219
PMCPMC3017199

What OpenQuestion holds

Textmetadata
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Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.