Generation and annotation of the DNA sequences of human chromosomes 2 and 4
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Summary
Extensive analyses confirm the underlying construction of the sequence, and expand the understanding of the structure and evolution of mammalian chromosomes, including gene deserts, segmental duplications and highly variant regions.
- Type
- article
- Published
- 2005-04-07
- Cited by
- 121
- References
- 52
- Access
- Open access
- OpenAlex
- https://openalex.org/W2032942231
- Semantic Scholar
- https://api.semanticscholar.org/CorpusID:4431946
Keywords
Biology, Genetics, Pseudogene, Chromosome 21, Chromosome 22
References
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- A physical map of the human genome
- Assessing the quality of finished genomic sequence.
- Genomic structure and evolution of the ancestral chromosome fusion site in 2q13-2q14.1 and paralogous regions on other human chromosomes.
- Integration of cytogenetic landmarks into the draft sequence of the human genome
- Regulatory potential scores from genome-wide three-way alignments of human, mouse, and rat.
- Number of CpG islands and genes in human and mouse.
- Mitochondrial DNA‐like sequences in the nucleus (NUMTs): Insights into our African origins and the mechanism of foreign DNA integration
- Human-specific duplication and mosaic transcripts: the recent paralogous structure of chromosome 22.
- Genomic organization of a new candidate tumor suppressor gene, LRP1B.
- InterProScan - an integration platform for the signature-recognition methods in InterPro
- Integration of telomere sequences with the draft human genome sequence
- Recent Segmental Duplications in the Human Genome
- ZAP-70 deficiency in an autosomal recessive form of severe combined immunodeficiency.
- Human-mouse alignments with BLASTZ.
- A map of human genome sequence variation containing 1.42 million single nucleotide polymorphisms
- Mutations of two P/WS homologues in hereditary nonpolyposis colon cancer
Cited by
- The procollagen type III, alpha 1 (COL3A1) gene first intron expresses poly‐A+ RNA corresponding to multiple ESTs and putative miRNAs
- Proviral load determination of HTLV-1 and HTLV-2 in patients' peripheral blood mononuclear cells by real-time PCR.
- Neural cell adhesion molecules belonging to the family of leucine-rich repeat proteins.
- Evolutionary and molecular genetics of regulatory alleles responsible for lactase persistence
- Régions de susceptibilité dans les remaniements du chromosome Y et mosaïcisme : facteurs de risque du développement sexuel anormal
- Design of a combinatorial DNA microarray for protein-DNA interaction studies
- Studio sull'origine e l'evoluzione del cromosoma 4 dell'uomo mediante la citogenetica molecolare comparata
- Optical diffraction-based silicon sensors for the detection of DNA sequences
- Investigation of genetic and developmental defects in the L11Jus8 mutant mouse
- Onconeural antibodies with special reference to anti-Yo
- A gene-based high-resolution comparative radiation hybrid map as a framework for genome sequence assembly of a bovine chromosome 6 region associated with QTL for growth, body composition, and milk performance traits
- A novel interstitial deletion of 2q22.3 q23.3 in a patient with dysmorphic features, epilepsy, aganglionosis, pure red cell aplasia, and skeletal malformations
- Of Protein Size and Genomes
- A novel locus of resistance to severe malaria in a region of ancient balancing selection
- Analysis of the DNA sequence and duplication history of human chromosome 15
- Mechanisms of Chromosome Number Evolution in Yeast
- 4q34.1–q35.2 deletion in a boy with phenotype resembling 22q11.2 deletion syndrome
- Novel transcripts discovered by mining genomic DNA from defined regions of bovine chromosome 6
- Variations of chromosomes 2 and 3 gene expression profiles among pulmonary telocytes, pneumocytes, airway cells, mesenchymal stem cells and lymphocytes
- Differential radio-sensitivities of human chromosomes 1 and 2 in one donor in interphase- and metaphase-spreads after 60Co γ-irradiation
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