C: Consensus Cancer Driver Gene Caller.

Next-generation sequencing has allowed identification of millions of somatic mutations in human cancer cells. A key challenge in interpreting cancer genomes is to distinguish drivers of cancer development among available genetic mutations. To address this issue, we present the first web-based application, consensus cancer driver gene caller (C), to identify the consensus driver genes using six different complementary strategies, i.

Robust authentication for paper-based text documents based on text watermarking technology.

Aiming at the problem of easy tampering and difficult integrity authentication of paper text documents, this paper proposes a robust content authentication method for printed documents based on text watermarking scheme resisting print-and-scan attack. Firstly, an authentication watermark signal sequence related to content of text document is generated based on the Logistic chaotic map model; then, the authentication watermark signal sequence is embedded into printed paper document by using a robust text watermarking scheme; finally, the watermark information is extracted from scanned image of paper document, and compared with the authentication watermark information calculated in real time by the text document content obtained by OCR technology, thereby performing content integrity authentication of the paper text documents. Experimental results show that our method can achieve the robust content integrity authentication of paper text documents, and can also accurately locate the tampering position.

[Expression of CD66c (CEACM6) in adult acute leukemia and its significance].

Objective: To explore the expression of CD66c (CEACM6) in adult acute leukemia and its significance.

Methods: Acute leukemia cell lines HL-60, K562, LCL721.221 and Jurkat were cultured in vitro.

Systematic analysis of head-to-head gene organization: evolutionary conservation and potential biological relevance.

Several "head-to-head" (or "bidirectional") gene pairs have been studied in individual experiments, but genome-wide analysis of this gene organization, especially in terms of transcriptional correlation and functional association, is still insufficient. We conducted a systematic investigation of head-to-head gene organization focusing on structural features, evolutionary conservation, expression correlation and functional association. Of the present 1,262, 1,071, and 491 head-to-head pairs identified in human, mouse, and rat genomes, respectively, pairs with 1- to 400-base pair distance between transcription start sites form the majority (62.

In silico discovery of human natural antisense transcripts.

Background: Several high-throughput searches for potential natural antisense transcripts (NATs) have been performed recently, but most of the reports were focused on cis type. A thorough in silico analysis of human transcripts will help expand our knowledge of NATs.

Results: We have identified 568 NATs from human RefSeq RNA sequences.

Cross-host evolution of severe acute respiratory syndrome coronavirus in palm civet and human.

The genomic sequences of severe acute respiratory syndrome coronaviruses from human and palm civet of the 2003/2004 outbreak in the city of Guangzhou, China, were nearly identical. Phylogenetic analysis suggested an independent viral invasion from animal to human in this new episode. Combining all existing data but excluding singletons, we identified 202 single-nucleotide variations.

Application of pseudo amino acid composition for predicting protein subcellular location: stochastic signal processing approach.

The function of a protein is closely correlated with its subcellular location. With the success of human genome project and the rapid increase in the number of newly found protein sequences entering into data banks, it is highly desirable to develop an automated method for predicting the subcellular location of proteins. The establishment of such a predictor will no doubt expedite the functionality determination of newly found proteins and the process of prioritizing genes and proteins identified by genomics efforts as potential molecular targets for drug design.

Identification of probable genomic packaging signal sequence from SARS-CoV genome by bioinformatics analysis.

Aim: To predict the probable genomic packaging signal of SARS-CoV by bioinformatics analysis. The derived packaging signal may be used to design antisense RNA and RNA interfere (RNAi) drugs treating SARS.

Methods: Based on the studies about the genomic packaging signals of MHV and BCoV, especially the information about primary and secondary structures, the putative genomic packaging signal of SARS-CoV were analyzed by using bioinformatic tools.

Putative hAPN receptor binding sites in SARS_CoV spike protein.

Aim: To obtain the information of ligand-receptor binding between the S protein of SARS-CoV and CD13, identify the possible interacting domains or motifs related to binding sites, and provide clues for studying the functions of SARS proteins and designing anti-SARS drugs and vaccines.

Methods: On the basis of comparative genomics, the homology search, phylogenetic analyses, and multi-sequence alignment were used to predict CD13 related interacting domains and binding sites in the S protein of SARS-CoV. Molecular modeling and docking simulation methods were employed to address the interaction feature between CD13 and S protein of SARS-CoV in validating the bioinformatics predictions.