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Institution

Wellcome Trust Sanger Institute

NonprofitCambridge, United Kingdom
About: Wellcome Trust Sanger Institute is a nonprofit organization based out in Cambridge, United Kingdom. It is known for research contribution in the topics: Population & Genome. The organization has 4009 authors who have published 9671 publications receiving 1224479 citations.


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Journal ArticleDOI
TL;DR: In this paper, the authors highlight the key technological developments that have enabled the growth in the data obtained from single-cell RNA-seq experiments, and highlight the advantages of using large numbers of cells.
Abstract: Measurement of the transcriptomes of single cells has been feasible for only a few years, but it has become an extremely popular assay. While many types of analysis can be carried out and various questions can be answered by single-cell RNA-seq, a central focus is the ability to survey the diversity of cell types in a sample. Unbiased and reproducible cataloging of gene expression patterns in distinct cell types requires large numbers of cells. Technological developments and protocol improvements have fueled consistent and exponential increases in the number of cells that can be studied in single-cell RNA-seq analyses. In this Perspective, we highlight the key technological developments that have enabled this growth in the data obtained from single-cell RNA-seq experiments.

661 citations

Journal ArticleDOI
John F. Peden1, Jemma C. Hopewell1, Danish Saleheen2, John C. Chambers3, Jorg Hager4, Nicole Soranzo5, Rory Collins1, John Danesh2, Paul Elliott3, Martin Farrall1, Kathy Stirrups5, Weihua Zhang3, Anders Hamsten6, Anders Hamsten7, Sarah Parish1, Mark Lathrop4, Hugh Watkins1, Robert Clarke1, Panos Deloukas5, Jaspal S. Kooner3, Anuj Goel1, Halit Ongen1, Rona J. Strawbridge7, Rona J. Strawbridge6, Simon Heath4, Anders Mälarstig6, Anders Mälarstig7, Anna Helgadottir1, John Öhrvik6, John Öhrvik7, Muhammed Murtaza5, Simon C. Potter5, Sarah E. Hunt5, Marc Delepine4, Shapour Jalilzadeh1, Tomas Axelsson8, Ann-Christine Syvänen8, Rhian Gwilliam5, Suzannah Bumpstead5, Emma Gray5, Sarah Edkins5, Lasse Folkersen6, Lasse Folkersen7, Theodosios Kyriakou1, Anders Franco-Cereceda7, Anders Gabrielsen7, Udo Seedorf9, Per Eriksson7, Per Eriksson6, Alison Offer1, Louise Bowman1, Peter Sleight1, Jane Armitage1, Richard Peto1, Gonçalo R. Abecasis10, Nabeel Ahmed, Mark J. Caulfield11, Peter Donnelly1, Philippe Froguel3, Angad S. Kooner, Mark I. McCarthy1, Nilesh J. Samani12, James Scott3, Joban Sehmi3, Angela Silveira6, Angela Silveira7, Mai-Lis Hellénius7, Ferdinand M. van't Hooft6, Ferdinand M. van't Hooft7, Gunnar O Olsson13, Stephan Rust9, Gerd Assmann9, Simona Barlera, Gianni Tognoni, Maria Grazia Franzosi, Pamela Linksted1, Fiona Green14, Asif Rasheed, Moazzam Zaidi, Nabi Shah, Maria Samuel, Nadeem Hayat Mallick, Muhammad Azhar, Khan Shah Zaman, Abdus Samad, M. Ishaq, Ali Raza Gardezi, Fazal-ur-Rehman Memon, Philippe M. Frossard, Tim D. Spector, Leena Peltonen5, Leena Peltonen15, Markku S. Nieminen, Juha Sinisalo, Veikko Salomaa, Samuli Ripatti15, Derrick A Bennett1, Karin Leander7, Bruna Gigante7, Ulf de Faire7, Silvia Pietri, Francesca Gori, Roberto Marchioli, Suthesh Sivapalaratnam16, John J.P. Kastelein16, Mieke D. Trip16, Eirini V. Theodoraki17, George V. Dedoussis17, Engert Jc18, Salim Yusuf19, Sonia S. Anand19 
TL;DR: Genome-wide association studies have identified 11 common variants convincingly associated with coronary artery disease (CAD), a modest number considering the apparent heritability of CAD(8) as mentioned in this paper.
Abstract: Genome-wide association studies have identified 11 common variants convincingly associated with coronary artery disease (CAD)(1-7), a modest number considering the apparent heritability of CAD(8). ...

654 citations

Journal ArticleDOI
Wesley C. Warren1, LaDeana W. Hillier1, Jennifer A. Marshall Graves2, Ewan Birney, Chris P. Ponting3, Frank Grützner4, Katherine Belov5, Webb Miller6, Laura Clarke7, Asif T. Chinwalla1, Shiaw Pyng Yang1, Andreas Heger3, Devin P. Locke1, Pat Miethke2, Paul D. Waters2, Frédéric Veyrunes8, Frédéric Veyrunes2, Lucinda Fulton1, Bob Fulton1, Tina Graves1, John W. Wallis1, Xose S. Puente9, Carlos López-Otín9, Gonzalo R. Ordóñez9, Evan E. Eichler10, Lin Chen10, Ze Cheng10, Janine E. Deakin2, Amber E. Alsop2, Katherine Thompson2, Patrick J. Kirby2, Anthony T. Papenfuss11, Matthew Wakefield11, Tsviya Olender12, Doron Lancet12, Gavin A. Huttley2, Arian F.A. Smit13, Andrew J Pask14, Peter Temple-Smith15, Peter Temple-Smith14, Mark A. Batzer16, Jerilyn A. Walker16, Miriam K. Konkel16, Robert S. Harris6, Camilla M. Whittington5, Emily S. W. Wong5, Neil J. Gemmell17, Emmanuel Buschiazzo17, Iris M. Vargas Jentzsch17, Angelika Merkel17, Juergen Schmitz18, Anja Zemann18, Gennady Churakov18, Jan Ole Kriegs18, Juergen Brosius18, Elizabeth P. Murchison19, Ravi Sachidanandam19, Carly Smith19, Gregory J. Hannon19, Enkhjargal Tsend-Ayush4, Daniel McMillan2, Rosalind Attenborough2, Willem Rens8, Malcolm A. Ferguson-Smith8, Christophe Lefevre14, Christophe Lefevre20, Julie A. Sharp14, Kevin R. Nicholas14, David A. Ray21, Michael Kube, Richard Reinhardt, Thomas H. Pringle, James Taylor22, Russell C. Jones, Brett Nixon, Jean Louis Dacheux23, Hitoshi Niwa, Yoko Sekita, Xiaoqiu Huang24, Alexander Stark25, Pouya Kheradpour25, Manolis Kellis25, Paul Flicek, Yuan Chen, Caleb Webber3, Ross C. Hardison, Joanne O. Nelson1, Kym Hallsworth-Pepin1, Kim D. Delehaunty1, Chris Markovic1, Patrick Minx1, Yucheng Feng1, Colin Kremitzki1, Makedonka Mitreva1, Jarret Glasscock1, Todd Wylie1, Patricia Wohldmann1, Prathapan Thiru1, Michael N. Nhan1, Craig Pohl1, Scott M. Smith1, Shunfeng Hou1, Marilyn B. Renfree14, Elaine R. Mardis1, Richard K. Wilson1 
08 May 2008-Nature
TL;DR: It is found that reptile and platypus venom proteins have been co-opted independently from the same gene families; milk protein genes are conserved despite platypuses laying eggs; and immune gene family expansions are directly related to platypUS biology.
Abstract: We present a draft genome sequence of the platypus, Ornithorhynchus anatinus This monotreme exhibits a fascinating combination of reptilian and mammalian characters For example, platypuses have a coat of fur adapted to an aquatic lifestyle; platypus females lactate, yet lay eggs; and males are equipped with venom similar to that of reptiles Analysis of the first monotreme genome aligned these features with genetic innovations We find that reptile and platypus venom proteins have been co-opted independently from the same gene families; milk protein genes are conserved despite platypuses laying eggs; and immune gene family expansions are directly related to platypus biology Expansions of protein, non-protein-coding RNA and microRNA families, as well as repeat elements, are identified Sequencing of this genome now provides a valuable resource for deep mammalian comparative analyses, as well as for monotreme biology and conservation

653 citations

Journal ArticleDOI
29 Jan 2015-Cell
TL;DR: It is reported that rapid evolution of enhancers is a universal feature of mammalian genomes and most of the recently evolved enhancers arise from ancestral DNA exaptation, rather than lineage-specific expansions of repeat elements.

653 citations

Journal ArticleDOI
TL;DR: This work has developed a cross-platform algorithm—Bayesian tool for methylation analysis (Batman)—for analyzing methylated DNA immunoprecipitation profiles generated using oligonucleotide arrays or next-generation sequencing, developed to provide a high-resolution whole-genome DNA methylation profile (DNA methylome) of a mammalian genome.
Abstract: DNA methylation is an indispensible epigenetic modification required for regulating the expression of mammalian genomes. Immunoprecipitation-based methods for DNA methylome analysis are rapidly shifting the bottleneck in this field from data generation to data analysis, necessitating the development of better analytical tools. In particular, an inability to estimate absolute methylation levels remains a major analytical difficulty associated with immunoprecipitation-based DNA methylation profiling. To address this issue, we developed a cross-platform algorithm-Bayesian tool for methylation analysis (Batman)-for analyzing methylated DNA immunoprecipitation (MeDIP) profiles generated using oligonucleotide arrays (MeDIP-chip) or next-generation sequencing (MeDIP-seq). We developed the latter approach to provide a high-resolution whole-genome DNA methylation profile (DNA methylome) of a mammalian genome. Strong correlation of our data, obtained using mature human spermatozoa, with those obtained using bisulfite sequencing suggest that combining MeDIP-seq or MeDIP-chip with Batman provides a robust, quantitative and cost-effective functional genomic strategy for elucidating the function of DNA methylation.

651 citations


Authors

Showing all 4058 results

NameH-indexPapersCitations
Nicholas J. Wareham2121657204896
Gonçalo R. Abecasis179595230323
Panos Deloukas162410154018
Michael R. Stratton161443142586
David W. Johnson1602714140778
Michael John Owen1601110135795
Naveed Sattar1551326116368
Robert E. W. Hancock15277588481
Julian Parkhill149759104736
Nilesh J. Samani149779113545
Michael Conlon O'Donovan142736118857
Jian Yang1421818111166
Christof Koch141712105221
Andrew G. Clark140823123333
Stylianos E. Antonarakis13874693605
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Performance
Metrics
No. of papers from the Institution in previous years
YearPapers
202317
202270
2021836
2020810
2019854
2018764