TIARA - Total Integrated Archive of short-Read and Array

Names

More detailed information about this field from each metasource. ×

TIARA - Total Integrated Archive of short-Read and Array

metasource: Nucleic Acid Research database catalogue
version: extracted_at: 2022-11-04T11:16:25.468657

---

TIARA

metasource: bio.tools
version: extracted_at: 2022-11-04T11:35:16.113737

---

tiara

metasource: bio.tools
version: extracted_at: 2022-11-04T11:35:16.113737

Close

Other names: TIARA, tiara

The Total Integrated Archive of short-Read and Array (TIARA) accumulates raw-level personal genomic data from whole genome next-generation sequencing (NGS) and comparative genomic hybridization (CGH) arrays. Initially, it contains 36 individual genomic data sets that have been analyzed and reported by the Genomic Medicine Institute (GMI) at Seoul National University (1,2,3). TIARA improves the accuracy of detecting personal genomic variations, such as SNPs, short indels, and structural variants (SVs). TIARA supports a user-friendly genome browser, which retrieves read-depths (RDs) and log2 ratios from NGS and CGH arrays, respectively. In addition, TIARA provides information on all genomic variants and the raw data, including short reads and feature-level CGH data, through anonymous file transfer protocol (FTP).

Webpage:

Publications:

Publications

More detailed information about this field from each metasource. ×

TIARA: a database for accurate analysis of multiple personal genomes based on cross-technology
PMID: 21051338

metasource: bio.tools
version: extracted_at: 2022-11-04T11:35:16.113737

---

http://nar.oxfordjournals.org/content/39/suppl_1/D883

metasource: Nucleic Acid Research database catalogue
version: extracted_at: 2022-11-04T11:16:25.468657

Close

• TIARA: a database for accurate analysis of multiple personal genomes based on cross-technology PubMed citations: 9.

  9 articles citing: TIARA: a database for accurate analysis of multiple personal genomes based on cross-technology

  ×

  Korean Genome Project: 1094 Korean personal genomes with clinical information. PMID:32766443

  ---

  Recessive C10orf2 mutations in a family with infantile-onset spinocerebellar ataxia, sensorimotor polyneuropathy, and myopathy. PMID:24816431

  ---

  Identification of CDH23 mutations in Korean families with hearing loss by whole-exome sequencing. PMID:24767429

  ---

  Whole-exome sequencing identifies MYO15A mutations as a cause of autosomal recessive nonsyndromic hearing loss in Korean families. PMID:23865914

  ---

  TIARA genome database: update 2013. PMID:23515433

  ---

  Clinical and histopathological study of Charcot-Marie-Tooth neuropathy with a novel S90W mutation in BSCL2. PMID:23142943

  ---

  Exploring the implications of INDELs in neuropsychiatric genetics: challenges and perspectives. PMID:22350990

  ---

  Extensive genomic and transcriptional diversity identified through massively parallel DNA and RNA sequencing of eighteen Korean individuals. PMID:21725310

  ---

  Sequencing technologies and genome sequencing. PMID:21698376
• http://nar.oxfordjournals.org/content/39/suppl_1/D883

Tags:

Tags

More detailed information about this field from each metasource. ×

human and other vertebrate genomes

metasource: Nucleic Acid Research database catalogue
version: extracted_at: 2022-11-04T11:16:25.468657

---

human genome databases, maps and viewers

metasource: Nucleic Acid Research database catalogue
version: extracted_at: 2022-11-04T11:16:25.468657

---

sequencing

metasource: bio.tools
version: extracted_at: 2022-11-04T11:35:16.113737

---

genomics

metasource: bio.tools
version: extracted_at: 2022-11-04T11:35:16.113737

---

dna polymorphism

metasource: bio.tools
version: extracted_at: 2022-11-04T11:35:16.113737

---

dna structural variation

metasource: bio.tools
version: extracted_at: 2022-11-04T11:35:16.113737

Close

human and other vertebrate genomes human genome, maps and viewers sequencing genomics dna polymorphism dna structural variation