Evidence map›Paper›PMID 11237011›Full record

ArticleNature2001

Initial sequencing and analysis of the human genome.

E S Lander, L M Linton, B Birren, C Nusbaum, M C Zody, J Baldwin, K Devon, K Dewar, M Doyle, W FitzHugh and 247 more

Erratum issued 3 registry-linked trialsAbstract read
PubMed Publisher
In one paragraph

Article in Nature, 2001. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. It is linked to 3 registered trials, which are not on this map. Cited by 8,819 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
8,819citing papers in PubMed, 2 pooled it
–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.

NCT00018889 recruitingnot on this map

Phenotype/Genotype Correlations in Movement Disorders

TypeobservationalSponsorNational Institute of Neurological Disorders and Stroke (NINDS)Ran2001Enrolled2,500ConditionsMovement Disorder
NCT01460186 nacompletednot on this mapstarted 2011, after this paper: background citation

Evaluation of the Predictive and Prognostic Value of Germ-line Polymorphisms in Patients With Metastatic Breast Cancer : a Multicenter Non-randomized Prospective Cohort Study

TypeinterventionalSponsorCentre Leon BerardRan2011 to 2017Enrolled1,000ConditionsBreast Cancer, MetastasisArmsBlood sample for genetic analysis (Identification of germ line genetic factors that influence the risk of metastatic breast cancer)
NCT02927158 recruitingnot on this mapstarted 2016, after this paper: background citation

Use of Whole Exome Sequencing/Whole Genome Sequencing in the Plain Communities

TypeobservationalSponsorUniversity of PittsburghRan2016 to 2040Enrolled300ConditionsUndiagnosed Disease
3 · Its place in the literature

Who cites it

8,819 citing papers in PubMed, 2 syntheses or guidelines pooled it.

  1. Pooled it
  2. Pooled it
  3. Article
  4. Review
  5. Article
  6. Conserved SINE and lineage-variable LINE-1 depletion at neurodevelopmental disorder promoters.Mammalian genome : official journal of the International Mammalian Genome Society · 2026
    Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Disruption of RNA metabolism and its impact on protein homeostasis.Philosophical transactions of the Royal Society of London. Series B, Biological sciences · 2026
    Review
  16. Cross-species incompatibilities offer new insights into the functional consequences of satellite DNA evolution.Chromosome research : an international journal on the molecular, supramolecular and evolutionary aspects of chromosome biology · 2026
    Review
  17. Article
  18. Article
  19. Article
  20. AcutebioRxiv : the preprint server for biology · 2026
    Article

8,759 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

257 authors.

E S LanderWhitehead Institute for Biomedical Research, Center for Genome Research, Cambridge, MA 02142, USA. lander@genome.wi.mit.edu
L M Linton
B Birren
C Nusbaum
M C Zody
J Baldwin
K Devon
K Dewar
M Doyle
W FitzHugh
R Funke
D Gage
K Harris
A Heaford
J Howland
L Kann
J Lehoczky
R LeVine
P McEwan
K McKernan
J Meldrim
J P Mesirov
C Miranda
W Morris
J Naylor
C Raymond
M Rosetti
R Santos
A Sheridan
C Sougnez
Y Stange-Thomann
N Stojanovic
A Subramanian
D Wyman
J Rogers
J Sulston
R Ainscough
S Beck
D Bentley
J Burton
C Clee
N Carter
A Coulson
R Deadman
P Deloukas
A Dunham
I Dunham
R Durbin
L French
D Grafham
S Gregory
T Hubbard
S Humphray
A Hunt
M Jones
C Lloyd
A McMurray
L Matthews
S Mercer
S Milne
J C Mullikin
A Mungall
R Plumb
M Ross
R Shownkeen
S Sims
R H Waterston
R K Wilson
L W Hillier
J D McPherson
M A Marra
E R Mardis
L A Fulton
A T Chinwalla
K H Pepin
W R Gish
S L Chissoe
M C Wendl
K D Delehaunty
T L Miner
A Delehaunty
J B Kramer
L L Cook
R S Fulton
D L Johnson
P J Minx
S W Clifton
T Hawkins
E Branscomb
P Predki
P Richardson
S Wenning
T Slezak
N Doggett
J F Cheng
A Olsen
S Lucas
C Elkin
E Uberbacher
M Frazier
R A Gibbs
D M Muzny
S E Scherer
J B Bouck
E J Sodergren
K C Worley
C M Rives
J H Gorrell
M L Metzker
S L Naylor
R S Kucherlapati
D L Nelson
G M Weinstock
Y Sakaki
A Fujiyama
M Hattori
T Yada
A Toyoda
T Itoh
C Kawagoe
H Watanabe
Y Totoki
T Taylor
J Weissenbach
R Heilig
W Saurin
F Artiguenave
P Brottier
T Bruls
E Pelletier
C Robert
P Wincker
D R Smith
L Doucette-Stamm
M Rubenfield
K Weinstock
H M Lee
J Dubois
A Rosenthal
M Platzer
G Nyakatura
S Taudien
A Rump
H Yang
J Yu
J Wang
G Huang
J Gu
L Hood
L Rowen
A Madan
S Qin
R W Davis
N A Federspiel
A P Abola
M J Proctor
R M Myers
J Schmutz
M Dickson
J Grimwood
D R Cox
M V Olson
R Kaul
C Raymond
N Shimizu
K Kawasaki
S Minoshima
G A Evans
M Athanasiou
R Schultz
B A Roe
F Chen
H Pan
J Ramser
H Lehrach
R Reinhardt
W R McCombie
M de la Bastide
N Dedhia
H Blöcker
K Hornischer
G Nordsiek
R Agarwala
L Aravind
J A Bailey
A Bateman
S Batzoglou
E Birney
P Bork
D G Brown
C B Burge
L Cerutti
H C Chen
D Church
M Clamp
R R Copley
T Doerks
S R Eddy
E E Eichler
T S Furey
J Galagan
J G Gilbert
C Harmon
Y Hayashizaki
D Haussler
H Hermjakob
K Hokamp
W Jang
L S Johnson
T A Jones
S Kasif
A Kaspryzk
S Kennedy
W J Kent
P Kitts
E V Koonin
I Korf
D Kulp
D Lancet
T M Lowe
A McLysaght
T Mikkelsen
J V Moran
N Mulder
V J Pollara
C P Ponting
G Schuler
J Schultz
G Slater
A F Smit
E Stupka
J Szustakowki
D Thierry-Mieg
J Thierry-Mieg
L Wagner
J Wallis
R Wheeler
A Williams
Y I Wolf
K H Wolfe
S P Yang
R F Yeh
F Collins
M S Guyer
J Peterson
A Felsenfeld
K A Wetterstrand
A Patrinos
M J Morgan
P de Jong
J J Catanese
K Osoegawa
H Shizuya
S Choi
Y J Chen
J Szustakowki
International Human Genome Sequencing Consortium

Funding

The Human Genome Sequencing CenterU54HG003273 · NHGRI · BAYLOR COLLEGE OF MEDICINE · PI GIBBS, RICHARD A · 2004 to 2015
$341.3M
6 · The paper itself

Abstract

The human genome holds an extraordinary trove of information about human development, physiology, medicine and evolution. Here we report the results of an international collaboration to produce and make freely available a draft sequence of the human genome. We also present an initial analysis of the data, describing some of the insights that can be gleaned from the sequence.

Indexed as

Genome, HumanHuman Genome ProjectSequence Analysis, DNAAnimalsChromosome MappingConserved SequenceCpG IslandsDatabases, FactualDNA Transposable ElementsDrug IndustryEvolution, MolecularForecastingGC Rich SequenceGene DuplicationGenesGenetic Diseases, InbornDNA Transposable ElementsProteinsProteomeRNA

Identifiers

PMID11237011

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

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.