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ReseqChip:从线粒体 DNA 序列组装中的 MitoChip 阵列中自动整合多个局部上下文探针数据。

ReseqChip: automated integration of multiple local context probe data from the MitoChip array in mitochondrial DNA sequence assembly.

机构信息

Institute of Functional Genomics, University of Regensburg, Josef-Engert-Str, 9, D-93053 Regensburg, Germany.

出版信息

BMC Bioinformatics. 2009 Dec 22;10:440. doi: 10.1186/1471-2105-10-440.

Abstract

BACKGROUND

The Affymetrix MitoChip v2.0 is an oligonucleotide tiling array for the resequencing of the human mitochondrial (mt) genome. For each of 16,569 nucleotide positions of the mt genome it holds two sets of four 25-mer probes each that match the heavy and the light strand of a reference mt genome and vary only at their central position to interrogate all four possible alleles. In addition, the MitoChip v2.0 carries alternative local context probes to account for known mtDNA variants. These probes have been neglected in most studies due to the lack of software for their automated analysis.

RESULTS

We provide ReseqChip, a free software that automates the process of resequencing mtDNA using multiple local context probes on the MitoChip v2.0. ReseqChip significantly improves base call rate and sequence accuracy. ReseqChip is available at http://code.open-bio.org/svnweb/index.cgi/bioperl/browse/bioperl-live/trunk/Bio/Microarray/Tools/.

CONCLUSIONS

ReseqChip allows for the automated consolidation of base calls from alternative local mt genome context probes. It thereby improves the accuracy of resequencing, while reducing the number of non-called bases.

摘要

背景

Affymetrix MitoChip v2.0 是一种用于人类线粒体(mt)基因组重测序的寡核苷酸平铺阵列。对于 mt 基因组的 16569 个核苷酸位置中的每一个,它都有两组四个 25 -mer 探针,每组探针分别与参考 mt 基因组的重链和轻链匹配,仅在中央位置有所不同,以检测所有四个可能的等位基因。此外,MitoChip v2.0 还携带替代的局部上下文探针,以解释已知的 mtDNA 变体。由于缺乏用于自动分析这些探针的软件,这些探针在大多数研究中都被忽略了。

结果

我们提供了 ReseqChip,这是一款免费软件,它使用 MitoChip v2.0 上的多个局部上下文探针自动进行 mtDNA 重测序。ReseqChip 显著提高了碱基调用率和序列准确性。ReseqChip 可在 http://code.open-bio.org/svnweb/index.cgi/bioperl/browse/bioperl-live/trunk/Bio/Microarray/Tools/ 获得。

结论

ReseqChip 允许从替代的局部 mt 基因组上下文探针中自动合并碱基调用。它提高了重测序的准确性,同时减少了未调用的碱基数量。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/da59/3087351/22ae418f8035/1471-2105-10-440-1.jpg

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