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Sequencing of idiopathic pulmonary fibrosis-related genes reveals independent single gene associations.

BMJ open respiratory research | 2014

Previous studies investigating a genetic basis for idiopathic pulmonary fibrosis (IPF) have focused on resequencing single genes in IPF kindreds or cohorts to determine the genetic contributions to IPF. None has investigated interactions among the candidate genes.

Pubmed ID: 25553246 RIS Download

Research resources used in this publication

None found

Antibodies used in this publication

None found

Associated grants

  • Agency: NHLBI NIH HHS, United States
    Id: RC2 HL102923
  • Agency: NHLBI NIH HHS, United States
    Id: UC2 HL102926
  • Agency: NHLBI NIH HHS, United States
    Id: UC2 HL103010
  • Agency: NHLBI NIH HHS, United States
    Id: RC2 HL102926
  • Agency: NHLBI NIH HHS, United States
    Id: R01 HL065174
  • Agency: NHLBI NIH HHS, United States
    Id: R01 HL082747
  • Agency: NHLBI NIH HHS, United States
    Id: RC2 HL102924
  • Agency: NHLBI NIH HHS, United States
    Id: UC2 HL102923
  • Agency: NCATS NIH HHS, United States
    Id: UL1 TR000448
  • Agency: NHLBI NIH HHS, United States
    Id: UC2 HL102924
  • Agency: NHLBI NIH HHS, United States
    Id: RC2 HL103010
  • Agency: NHLBI NIH HHS, United States
    Id: RC2 HL102925
  • Agency: NHLBI NIH HHS, United States
    Id: UC2 HL102925
  • Agency: NHLBI NIH HHS, United States
    Id: K12 HL089968
  • Agency: NHLBI NIH HHS, United States
    Id: P50 HL084922

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This is a list of tools and resources that we have found mentioned in this publication.


NHLBI Exome Sequencing Project (ESP) (tool)

RRID:SCR_012761

The goal of the project is to discover novel genes and mechanisms contributing to heart, lung and blood disorders by pioneering the application of next-generation sequencing of the protein coding regions of the human genome across diverse, richly-phenotyped populations and to share these datasets and findings with the scientific community to extend and enrich the diagnosis, management and treatment of heart, lung and blood disorders. The groups participating and collaborating in the NHLBI GO ESP include: Seattle GO - University of Washington, Seattle, WA Broad GO - Broad Institute of MIT and Harvard, Cambridge, MA WHISP GO - Ohio State University Medical Center, Columbus, OH Lung GO - University of Washington, Seattle, WA WashU GO - Washington University, St. Louis, MO Heart GO - University of Virginia Health System, Charlottesville, VA ChargeS GO - University of Texas Health Sciences Center at Houston

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REDCap (tool)

RRID:SCR_003445

Web application that allows users to build and manage online surveys and databases. Using REDCap's stream-lined process for rapidly developing projects, you may create and design projects using 1) the online method from your web browser using the Online Designer; and/or 2) the offline method by constructing a "data dictionary" template file in Microsoft Excel, which can be later uploaded into REDCap. Both surveys and databases (or a mixture of the two) can be built using these methods. REDCap provides audit trails for tracking data manipulation and user activity, as well as automated export procedures for seamless data downloads to Excel, PDF, and common statistical packages (SPSS, SAS, Stata, R). Also included are a built-in project calendar, a scheduling module, ad hoc reporting tools, and advanced features, such as branching logic, file uploading, and calculated fields. REDCap has a quick and easy software installation process, so that you can get REDCap running and fully functional in a matter of minutes. Several language translations have already been compiled for REDCap (e.g. Chinese, French, German, Portuguese), and it is anticipated that other languages will be available in full versions of REDCap soon. The REDCap Shared Library is a repository for REDCap data collection instruments and forms that can be downloaded and used by researchers at REDCap partner institutions.

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SPLINTER (tool)

RRID:SCR_005826

Software that detects and quantifies short IN/DELs as well as single nucleotide substitutions in pooled-DNA samples.

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SIFT (tool)

RRID:SCR_012813

Data analysis service to predict whether an amino acid substitution affects protein function based on sequence homology and the physical properties of amino acids. SIFT can be applied to naturally occurring nonsynonymous polymorphisms and laboratory-induced missense mutations. (entry from Genetic Analysis Software) Web service is also available.

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