Literature DB >> 19360699

An overview of custom array sequencing.

Prachi Kothiyal1, Stephanie Cox, Jonathan Ebert, Bruce J Aronow, John H Greinwald, Heidi L Rehm.   

Abstract

This unit provides an overview of oligo hybridization-based resequencing and a wide range of considerations for implementing the technology and analyzing the resulting data. The specific technology discussed is the Affymetrix GeneChip CustomSeq Resequencing Array platform. Concepts related to array design, experimental protocols, and base-calling using existing algorithms are presented. Details that should be evaluated during development of sequence tiling, target amplification, and PCR protocols are addressed. An overview of the Affymetrix GeneChip Sequence Analysis Software (GSEQ) is provided, along with factors that influence base-calling coverage and accuracy. Also outlined are performance measures that can be used to characterize base-calling with resequencing arrays, as well as factors known to affect their performance. Limitations associated with detection of insertions and deletions (indels) are discussed, with empirical data from our experiments used to outline possible approaches to indel detection. Critical topics in the design, implementation, and analysis of targeted sequencing arrays not previously discussed in detail are highlighted.

Entities:  

Mesh:

Year:  2009        PMID: 19360699      PMCID: PMC4528186          DOI: 10.1002/0471142905.hg0717s61

Source DB:  PubMed          Journal:  Curr Protoc Hum Genet        ISSN: 1934-8258


  2 in total

1.  High-throughput variation detection and genotyping using microarrays.

Authors:  D J Cutler; M E Zwick; M M Carrasquillo; C T Yohn; K P Tobin; C Kashuk; D J Mathews; N A Shah; E E Eichler; J A Warrington; A Chakravarti
Journal:  Genome Res       Date:  2001-11       Impact factor: 9.043

Review 2.  High density synthetic oligonucleotide arrays.

Authors:  R J Lipshutz; S P Fodor; T R Gingeras; D J Lockhart
Journal:  Nat Genet       Date:  1999-01       Impact factor: 38.330

  2 in total
  12 in total

Review 1.  Evolving molecular diagnostics for familial cardiomyopathies: at the heart of it all.

Authors:  Thomas E Callis; Brian C Jensen; Karen E Weck; Monte S Willis
Journal:  Expert Rev Mol Diagn       Date:  2010-04       Impact factor: 5.225

2.  Resequencing and association analysis of the KALRN and EPHB1 genes and their contribution to schizophrenia susceptibility.

Authors:  Itaru Kushima; Yukako Nakamura; Branko Aleksic; Masashi Ikeda; Yoshihito Ito; Tomoko Shiino; Tomo Okochi; Yasuhisa Fukuo; Hiroshi Ujike; Michio Suzuki; Toshiya Inada; Ryota Hashimoto; Masatoshi Takeda; Kozo Kaibuchi; Nakao Iwata; Norio Ozaki
Journal:  Schizophr Bull       Date:  2010-11-01       Impact factor: 9.306

3.  Hybridisation-based resequencing of 17 X-linked intellectual disability genes in 135 patients reveals novel mutations in ATRX, SLC6A8 and PQBP1.

Authors:  Lars R Jensen; Wei Chen; Bettina Moser; Bettina Lipkowitz; Christopher Schroeder; Luciana Musante; Andreas Tzschach; Vera M Kalscheuer; Ilaria Meloni; Martine Raynaud; Hilde van Esch; Jamel Chelly; Arjan P M de Brouwer; Anna Hackett; Sigrun van der Haar; Wolfram Henn; Jozef Gecz; Olaf Riess; Michael Bonin; Richard Reinhardt; Hans-Hilger Ropers; Andreas W Kuss
Journal:  Eur J Hum Genet       Date:  2011-01-26       Impact factor: 4.246

4.  Juvenile myelomonocytic leukemia-associated variants are associated with neo-natal lethal Noonan syndrome.

Authors:  Heather Mason-Suares; Diana Toledo; Jean Gekas; Katherine A Lafferty; Naomi Meeks; M Cristina Pacheco; David Sharpe; Thomas E Mullen; Matthew S Lebo
Journal:  Eur J Hum Genet       Date:  2017-01-18       Impact factor: 4.246

5.  Revisiting the genetic diversity of emerging hantaviruses circulating in Europe using a pan-viral resequencing microarray.

Authors:  Claudia Filippone; Guillaume Castel; Séverine Murri; Myriam Ermonval; Misa Korva; Tatjana Avšič-Županc; Tarja Sironen; Olli Vapalahati; Lorraine M McElhinney; Rainer G Ulrich; Martin H Groschup; Valérie Caro; Frank Sauvage; Sylvie van der Werf; Jean-Claude Manuguerra; Antoine Gessain; Philippe Marianneau; Noël Tordo
Journal:  Sci Rep       Date:  2019-08-27       Impact factor: 4.379

Review 6.  Novel sequencing-based strategies for high-throughput discovery of genetic mutations underlying inherited antibody deficiency disorders.

Authors:  Hong-Ying Wang; Ashish Jain
Journal:  Curr Allergy Asthma Rep       Date:  2011-10       Impact factor: 4.806

7.  ATM mutations uniformly lead to ATM dysfunction in chronic lymphocytic leukemia: application of functional test using doxorubicin.

Authors:  Veronika Navrkalova; Ludmila Sebejova; Jana Zemanova; Jana Kminkova; Blanka Kubesova; Jitka Malcikova; Marek Mraz; Jana Smardova; Sarka Pavlova; Michael Doubek; Yvona Brychtova; David Potesil; Veronika Nemethova; Jiri Mayer; Sarka Pospisilova; Martin Trbusek
Journal:  Haematologica       Date:  2013-04-12       Impact factor: 9.941

8.  A novel custom resequencing array for dilated cardiomyopathy.

Authors:  Rebekah S Zimmerman; Stephanie Cox; Neal K Lakdawala; Allison Cirino; Debora Mancini-DiNardo; Eugene Clark; Annette Leon; Elizabeth Duffy; Emily White; Samantha Baxter; Manal Alaamery; Lisa Farwell; Scott Weiss; Christine E Seidman; Jonathan G Seidman; Carolyn Y Ho; Heidi L Rehm; Birgit H Funke
Journal:  Genet Med       Date:  2010-05       Impact factor: 8.822

Review 9.  Clinical genetic testing of periodic fever syndromes.

Authors:  Annalisa Marcuzzi; Elisa Piscianz; Giulio Kleiner; Alberto Tommasini; Giovanni Maria Severini; Lorenzo Monasta; Sergio Crovella
Journal:  Biomed Res Int       Date:  2013-01-01       Impact factor: 3.411

10.  SNP Discovery through Next-Generation Sequencing and Its Applications.

Authors:  Santosh Kumar; Travis W Banks; Sylvie Cloutier
Journal:  Int J Plant Genomics       Date:  2012-11-22
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