(Q51345578)

4 April 2018

title

Mixed sequence reader: a program for analyzing DNA sequences with heterozygous base calling. (English)

1 reference

4 April 2018

1 reference

9

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4 April 2018

author name string

Chun-Tien Chang

1

1 reference

4 April 2018

Chi-Neu Tsai

2

1 reference

4 April 2018

Chuan Yi Tang

3

1 reference

4 April 2018

Chun-Houh Chen

4

1 reference

4 April 2018

Jang-Hau Lian

5

1 reference

4 April 2018

Chi-Yu Hu

6

1 reference

4 April 2018

Chia-Lung Tsai

7

1 reference

4 April 2018

Angel Chao

8

1 reference

4 April 2018

Tzu-Hao Wang

10

1 reference

4 April 2018

Yun-Shien Lee

11

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4 April 2018

language of work or name

English

0 references

publication date

18 June 2012

1 reference

4 April 2018

The Scientific World Journal

published in

1 reference

4 April 2018

volume

2012

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4 April 2018

page(s)

365104

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4 April 2018

Creative Commons Attribution 3.0 Unported

copyright license

start time

1 January 2012

1 reference

April 2022 Public Data File from Crossref

copyright status

copyrighted

1 reference

April 2022 Public Data File from Crossref

cites work

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Pathway analysis of breast cancer genome-wide association study highlights three pathways and one canonical signaling cascade

22 May 2018

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22 May 2018

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Origins and functional impact of copy number variation in the human genome

22 May 2018

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22 May 2018

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Decoding of superimposed traces produced by direct sequencing of heterozygous indels

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22 May 2018

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22 May 2018

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22 May 2018

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22 May 2018

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22 May 2018

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22 May 2018

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22 May 2018

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22 May 2018

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22 May 2018

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Gene copy number regulates the production of the human chemokine CCL3-L1

22 May 2018

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22 May 2018

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Relative quantification of 40 nucleic acid sequences by multiplex ligation-dependent probe amplification

22 May 2018

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Validation of the AMPFlSTR SGM plus system for use in forensic casework

22 May 2018

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Both copy number and sequence variations affect expression of human DEFB4.

22 May 2018

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CGcgh: a tool for molecular karyotyping using DNA microarray-based comparative genomic hybridization (array-CGH).

14 August 2018

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High-resolution mapping of the 8p23.1 beta-defensin cluster reveals strictly concordant copy number variation of all genes.

14 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3385616

Human papillomavirus typing with a polymerase chain reaction-based genotyping array compared with type-specific PCR.

14 August 2018

1 reference

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Copy number polymorphisms are not a common feature of innate immune genes

14 August 2018

1 reference

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Human papillomavirus in oral leukoplakia is no prognostic indicator of malignant transformation

14 August 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/22778697

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Forensic analysis of autosomal STR markers using Pyrosequencing

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/22778697

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

STR primer concordance study

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/22778697

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1100/2012/365104

1 reference

4 April 2018

PMC publication ID

3385616

1 reference

4 April 2018

PubMed publication ID

22778697

1 reference

4 April 2018