Literature DB >> 17488757

Madeline 2.0 PDE: a new program for local and web-based pedigree drawing.

Edward H Trager1, Ritu Khanna, Adrian Marrs, Lawrence Siden, Kari E H Branham, Anand Swaroop, Julia E Richards.   

Abstract

UNLABELLED: The Madeline 2.0 Pedigree Drawing Engine (PDE) is a pedigree drawing program for use in linkage and family-based association studies. The program is designed to handle large and complex pedigrees with an emphasis on readability and aesthetics. For complex pedigrees, we use a hybrid algorithm in which consanguinous loops are drawn as cyclic graphs whenever possible, but we resort to acyclic graphs when matings can no longer be connected without line crossings. A similar hybrid approach is used to avoid line crossings for matings between distant descendants of different founding groups. Written in object-oriented C++ and released under the GNU General Public License (GPL), Madeline 2.0 PDE reads input files specified on the command line and generates pedigree drawings without user interaction. Pedigree output in scalable vector graphics (SVG) format can be viewed in browsers with native SVG rendering support or in vector graphics editors. We provide an easy-to-use public web service, which is experimental and still under development. AVAILABILITY: http://kellogg.umich.edu/madeline.

Mesh:

Year:  2007        PMID: 17488757     DOI: 10.1093/bioinformatics/btm242

Source DB:  PubMed          Journal:  Bioinformatics        ISSN: 1367-4803            Impact factor:   6.937


  14 in total

1.  A system for exact and approximate genetic linkage analysis of SNP data in large pedigrees.

Authors:  Mark Silberstein; Omer Weissbrod; Lars Otten; Anna Tzemach; Andrei Anisenia; Oren Shtark; Dvir Tuberg; Eddie Galfrin; Irena Gannon; Adel Shalata; Zvi U Borochowitz; Rina Dechter; Elizabeth Thompson; Dan Geiger
Journal:  Bioinformatics       Date:  2012-11-18       Impact factor: 6.937

2.  The kinship2 R package for pedigree data.

Authors:  Jason P Sinnwell; Terry M Therneau; Daniel J Schaid
Journal:  Hum Hered       Date:  2014-07-29       Impact factor: 0.444

3.  Rare Inherited and De Novo CNVs Reveal Complex Contributions to ASD Risk in Multiplex Families.

Authors:  Virpi M Leppa; Stephanie N Kravitz; Christa Lese Martin; Joris Andrieux; Cedric Le Caignec; Dominique Martin-Coignard; Christina DyBuncio; Stephan J Sanders; Jennifer K Lowe; Rita M Cantor; Daniel H Geschwind
Journal:  Am J Hum Genet       Date:  2016-08-25       Impact factor: 11.025

4.  Helium: visualization of large scale plant pedigrees.

Authors:  Paul D Shaw; Martin Graham; Jessie Kennedy; Iain Milne; David F Marshall
Journal:  BMC Bioinformatics       Date:  2014-08-01       Impact factor: 3.169

5.  The novel homozygous KCNJ10 c.986T>C (p.(Leu329Pro)) variant is pathogenic for the SeSAME/EAST homologue in Malinois dogs.

Authors:  Mario Van Poucke; Kimberley Stee; Sofie F M Bhatti; An Vanhaesebrouck; Leslie Bosseler; Luc J Peelman; Luc Van Ham
Journal:  Eur J Hum Genet       Date:  2016-12-14       Impact factor: 4.246

6.  genoDraw: A Web Tool for Developing Pedigree Diagrams Using the Standardized Human Pedigree Nomenclature Integrated with Biomedical Vocabularies.

Authors:  Luciano Garcia-Giordano; Sergio Paraiso-Medina; Raul Alonso-Calvo; Francisco Javier Fernández-Martínez; Victor Maojo
Journal:  AMIA Annu Symp Proc       Date:  2020-03-04

7.  PedWiz: a web-based tool for pedigree informatics.

Authors:  Yeunjoo E Song; Robert C Elston
Journal:  Front Genet       Date:  2013-09-25       Impact factor: 4.599

Review 8.  Genealogical data in population medical genetics: Field guidelines.

Authors:  Fernando A Poletta; Ieda M Orioli; Eduardo E Castilla
Journal:  Genet Mol Biol       Date:  2014-03       Impact factor: 1.771

9.  Pedimap: software for the visualization of genetic and phenotypic data in pedigrees.

Authors:  Roeland E Voorrips; Marco C A M Bink; W Eric van de Weg
Journal:  J Hered       Date:  2012-10-19       Impact factor: 2.645

10.  Exome Sequencing and Gene Prioritization Correct Misdiagnosis in a Chinese Kindred with Familial Amyloid Polyneuropathy.

Authors:  Hui Chen; Xueya Zhou; Jing Wang; Xi Wang; Liyang Liu; Shinan Wu; Tengyan Li; Si Chen; Jingwen Yang; Pak Chung Sham; Guangming Zhu; Xuegong Zhang; Binbin Wang
Journal:  Sci Rep       Date:  2016-05-23       Impact factor: 4.379

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