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ChromasPro具体功能
打开Applied Biosystems .ab1, Staden Chromatogram (SCF and ZTR), 454 SFF, FASTA, FASTQ, EMBL, GenBank, SwissProt, GenPept, GCG RSF和纯文本格式中的序列。
以.ab1, .scf, .fasta 和.fastq格式保存序列。
使用图形界面组装重叠序列,生成一致性并**模糊性进行编辑。
使用高质量数据自动去除低质量序列以改进序列组装。
ChromasPro is suitable for DNA sequence assembly projects up to a few megabases, and basic sequence editing and analysis. It is able to assemble data from Sanger sequencers such as ABI, and 454 and Illumina next-generation sequencers, with up to 1,000,000 sequences if 8 Gb RAM is available. ChromasPro has the following features:
![ChromasPro入门教程](//l.b2b168.com/2019/07/18/10/201907181030352586494.jpg)
Fixed a reference sequence rendering issue in the contig editor when zoomed in.
BLAST searches now include the option of submitting directly to the server to avoid the URL length limit with web browsers. Results still open in the default browser.
The lengths of contig consensus sequences listed in the project now exclude gaps.
![ChromasPro入门教程](//l.b2b168.com/2019/07/18/10/201907181030385050684.jpg)
Changes from version 1.9.9.1 beta:
![ChromasPro入门教程](//l.b2b168.com/2019/07/19/15/201907191511177039654.jpg)
Added 32-bit version to installer.
Added an option to show statistical information for a contig.
Pressing the up arrow in row one of the alignment moves the cursor to the consensus.
Shift+mou*heel scrolls the alignment or aligned chromatograms.
Fixed bug which prevented consensus recalculation after removing an aligned sequence at the 5′ end.
Fixed bug which could leave unnecessary gaps if more than 1 base was deleted from an aligned sequence at once.
Fixed rare error when undoing a large consensus deletion at the 5′ end spanning the entire first aligned sequence.
Fixed the scroll range sometimes initially being a few bases short.
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