NOVELTIES
OECD Series on Principles of Good Laboratory Practice and Compliance Monitoring. List of documents to be retrieved in pdf format. Registration not required.
Click here for more informationsPublished on 2010-07-26 06:37:22
The National Comprehensive Cancer Network® (NCCN®) is a not-for-profit alliance of 31 leading cancer centers devoted to patient care, research, and education. NCCN is dedicated to improving and facilitating quality, effective, equitable, and accessible cancer care so all patients can live better lives. Registration not required.
Click here for more informationsPublished on 2010-07-26 05:55:57
PROMO (from Universitat Politècnica de Catalunya) from is a virtual laboratory for the identification of putative transcription factor binding sites (TFBS) in DNA sequences from a species or groups of species of interest. TFBS defined in the TRANSFAC database are used to construct specific binding site weight matrices for TFBS prediction. The user can inspect the result of the search through a graphical interface and downloadable text files. PROMO is using version 8.3 of TRANSFAC. Registration not required.
Click here for more informationsPublished on 2010-07-25 02:52:23
The NIOSH Pocket Guide to Chemical Hazards (NPG) presents key information and data in abbreviated or tabular form for chemicals or substance groupings (e.g. cyanides, fluorides, manganese compounds) that are found in the work environment. Registration not required.
Click here for more informationsPublished on 2010-07-24 05:55:23
The Integrated Risk Information System (IRIS) is a human health assessment program that evaluates quantitative and qualitative risk information on effects that may result from exposure to environmental contaminants. The information in IRIS is intended for those without extensive training in toxicology, but with some knowledge of health sciences. Registration not required.
Click here for more informationsPublished on 2010-07-24 05:28:45
Rapid access to internationally peer reviewed information on chemicals commonly used throughout the world, which may also occur as contaminants in the environment and food. It consolidates information from a number of intergovernmental organizations whose goal it is to assist in the sound management of chemicals. Registration not required.
Click here for more informationsPublished on 2010-07-24 05:27:16
Information & treatment con various cancer types Registration not required.
Click here for more informationsPublished on 2010-07-24 05:23:16
NCCN Clinical Practice Guidelines in Oncology (NCCN Guidelines™) Registration required.
Click here for more informationsPublished on 2010-07-24 05:17:19
ClustalW2 is a general purpose multiple sequence alignment program for DNA or proteins. The online version is hosted by EMBL. It produces biologically meaningful multiple sequence alignments of divergent sequences. It calculates the best match for the selected sequences, and lines them up so that the identities, similarities and differences can be seen. Registration not required.
Click here for more informationsPublished on 2010-07-11 00:00:00
PRALINE is a multiple sequence alignment program with many options to optimise the information for each of the input sequences; e.g. homology-extended alignment, predicted secondary structure and/or transmembrane structure information and iteration capabilities. Registration not required.
Click here for more informationsPublished on 2010-07-11 00:00:00
GeConT (Gene Context Tool) is a web interface designed to visualize genome context of a gene or a group of genes and their orthologs in all the completely sequenced genomes. The graphical information of GeConT can be used to analyze genome annotation, functional ortholog identification or to verify the genomic context congruence of any set of genes that share a common property. Registration not required.
Click here for more informationsPublished on 2010-07-11 00:00:00
Multiple Sequence Alignment is the arrangement of several protein or nucleic acid sequences with postulated gaps so that similar residues (in one-letter code) are juxtaposed. Registration not required.
Click here for more informationsPublished on 2010-07-11 00:00:00
The Wise2 form compares a protein sequence to a genomic DNA sequence, allowing for introns and frameshifting errors. Registration not required.
Click here for more informationsPublished on 2010-07-11 00:00:00
SDS (siRNA Design Software) is a software tool that helps to design siRNAs for silencing gene expression. The tool takes an mRNA sequence and makes use of existing design tools to output a set of candidates. These candidates are then filtered based on the secondary structure. With the following features: It provides a unified platform for using existing software. It compares the output of existing software. It enhances the existing software by filtering ineffective siRNAs based on secondary structure. Registration not required.
Click here for more informationsPublished on 2010-07-10 00:00:00
ESPript, 'Easy Sequencing in PostScript', is a program which renders sequence similarities and secondary structure information from aligned sequences for analysis and publication purpose. Registration not required.
Click here for more informationsPublished on 2010-06-28 00:00:00
H-BloX is a web-based JavaScript application that allows one to calculate and visualize the Shannon information or the relative entropy (Kullback-Leibler distance) of sequence alignment blocks. Various residue alphabets may be defined and useful modifications of the alignment block and the alphabet can be applied before calculation. Registration not required.
Click here for more informationsPublished on 2010-06-28 00:00:00
PipMaker computes alignments of similar regions in two DNA sequences. The resulting alignments are summarized with a ``percent identity plot'', or ``pip'' for short. MultiPipMaker allows the user to see relationships among more than two sequences. All pairwise alignments with the first sequence are computed and then returned as interleaved pips. Moreover, MultiPipMaker can be requested to compute a true multiple alignment of the input sequences and return a nucleotide-level view of the results. Registration not required.
Click here for more informationsPublished on 2010-06-28 00:00:00
Java Dot Plot Alignments (JDotter) is a platform-independent Java interactive interface for the Linux version of Dotter, a widely used program for generating dotplots of large DNA or protein sequences. JDotter runs as a client-server application and can send new sequences to the Dotter program for alignment as well as rapidly access a repository of preprocessed dotplots. JDotter also interfaces with a sequence database or file system to display supplementary feature data. Thus, JDotter greatly simplifies access to dotplot data in laboratories that deal with large numbers of genomes and have a multi-platform organization. Registration not required.
Click here for more informationsPublished on 2010-06-28 00:00:00
YASS is a genomic similarity search tool, for nucleic (DNA/RNA) sequences in fasta or plain text format (it produces local pairwise alignments). Registration not required.
Click here for more informationsPublished on 2010-06-28 00:00:00
Dotlet is a program for comparing sequences by the diagonal plot method. It is designed to be platform-independent and to run in a Web browser, thus enabling the majority of researchers to use it. Registration not required.
Click here for more informationsPublished on 2010-06-28 00:00:00
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