AbstractIn using pooling designs to identify clones containing a specific subsequence called positive clones, sometimes there exist nonpositive clones which can cancel the effect of positive clones. Various models have been studied which differ in the power of cancellation. Although the various models pose interesting mathematical problems, and ingenious constructions of pooling designs have been proposed, in practice we rarely are sure about the true model and thus about which pooling design to use. In this paper we give a pooling design which fits all inhibitor models, and does not use more tests than in the more specific models. In particular, we obtain a 1-round pooling design for the k-inhibitor model for which only sequential designs ...
The complex molecular networks in the cell can give rise to surprising interactions: gene deletions ...
AbstractConsider a collection of objects, some of which may be “bad,” and a test which determines wh...
Abstract Background A key goal of drug discovery is t...
AbstractIn using pooling designs to identify clones containing a specific subsequence called positiv...
Pooling designs are used in clone library screening to ef ciently distinguish positive clones from ...
In this paper, we study the pooling experiments for screening clone maps. Clones are overlapped and ...
We describe efficient methods for screening clone libraries, based on pooling schemes that we call "...
AbstractGiven n clones with some positive ones, the problem of DNA screening is to identify all posi...
AbstractMacula proposed a novel construction of pooling designs which can effectively identify posit...
AbstractWe show that Macula's claim of a Hamming distance 4 between any two candidate sets of positi...
AbstractPooling designs are standard experimental tools in many biotechnical applications. It is wel...
This is the final report of a three-year, Laboratory Directed Research and Development (LDRD) projec...
High-throughput experiments provide a fast, automated way to obtain massive amounts of information a...
We discuss pooling methods of mutation detection for identifying rare mutations. We provide mathemat...
BACKGROUND: In binary high-throughput screening projects where the goal is the identification of low...
The complex molecular networks in the cell can give rise to surprising interactions: gene deletions ...
AbstractConsider a collection of objects, some of which may be “bad,” and a test which determines wh...
Abstract Background A key goal of drug discovery is t...
AbstractIn using pooling designs to identify clones containing a specific subsequence called positiv...
Pooling designs are used in clone library screening to ef ciently distinguish positive clones from ...
In this paper, we study the pooling experiments for screening clone maps. Clones are overlapped and ...
We describe efficient methods for screening clone libraries, based on pooling schemes that we call "...
AbstractGiven n clones with some positive ones, the problem of DNA screening is to identify all posi...
AbstractMacula proposed a novel construction of pooling designs which can effectively identify posit...
AbstractWe show that Macula's claim of a Hamming distance 4 between any two candidate sets of positi...
AbstractPooling designs are standard experimental tools in many biotechnical applications. It is wel...
This is the final report of a three-year, Laboratory Directed Research and Development (LDRD) projec...
High-throughput experiments provide a fast, automated way to obtain massive amounts of information a...
We discuss pooling methods of mutation detection for identifying rare mutations. We provide mathemat...
BACKGROUND: In binary high-throughput screening projects where the goal is the identification of low...
The complex molecular networks in the cell can give rise to surprising interactions: gene deletions ...
AbstractConsider a collection of objects, some of which may be “bad,” and a test which determines wh...
Abstract Background A key goal of drug discovery is t...