ArticleGenome biology2007
A BAC clone fingerprinting approach to the detection of human genome rearrangements.
Article in Genome biology, 2007. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
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Who cites it
7 citing papers in PubMed.
- A Leap Forward Towards Unraveling Newer Anti-infective Agents from an Unconventional Source: a Draft Genome Sequence Illuminating the Future Promise of Marine Heterotrophic Bacillus sp. Against Drug-Resistant Pathogens.Marine biotechnology (New York, N.Y.) · 2021Article
- LTC: a novel algorithm to improve the efficiency of contig assembly for physical mapping in complex genomes.BMC bioinformatics · 2010Article
- Somatic mutations altering EZH2 (Tyr641) in follicular and diffuse large B-cell lymphomas of germinal-center origin.Nature genetics · 2010Article
- Circos: an information aesthetic for comparative genomics.Genome research · 2009Article
- Smoking-related genomic signatures in non-small cell lung cancer.American journal of respiratory and critical care medicine · 2008Article
- Optimal pooling for genome re-sequencing with ultra-high-throughput short-read technologies.Bioinformatics (Oxford, England) · 2008Article
- A sequence-based survey of the complex structural organization of tumor genomes.Genome biology · 2008Article
Corrections and comments
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Authors and funding
16 authors.
Funding
Abstract
We present a method, called fingerprint profiling (FPP), that uses restriction digest fingerprints of bacterial artificial chromosome clones to detect and classify rearrangements in the human genome. The approach uses alignment of experimental fingerprint patterns to in silico digests of the sequence assembly and is capable of detecting micro-deletions (1-5 kb) and balanced rearrangements. Our method has compelling potential for use as a whole-genome method for the identification and characterization of human genome rearrangements.
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Registered trials
Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.