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New Generation Sequencer Data Analysis

Various NGS indluding Solexa, SOLiD and 454, data analysis tools are provided. These tools can handle numerous number of short reads generated from these next generation sequencers such as Illumina, Applied Biosystems and Roche. These tools are mainly implemented on GenomeTraveler. MetaGenomeGAMBLER also provides some of such tools.

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1 NGSフラグメントショートリードの参照ゲノムへのマッピング Monday, 13 June 2011 GT Developer 2833
2 ペアエンド配列の参照ゲノムへのマッピング Wednesday, 26 January 2011 Administrator 2977
3 Short Readのマッピング結果からSNPsを検出する Wednesday, 26 January 2011 Administrator 2727
4 参照ゲノム全域にわたるCoverage DepthをCSV形式でファイル出力する Wednesday, 26 January 2011 Administrator 2667
5 ABI SOLiDのカラースペース(CSFastA)で記述された配列ファイルを参照ゲノムにマッピングする Saturday, 22 January 2011 Administrator 2999

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