UNDERSTANDINGS / APPLICATIONS / SKILLS / NATURE OF SCIENCE
3.1.U1: A gene is a heritable factor that consists of a length of DNA and influences a specific characteristic
3.1.U2: A gene occupies a specific position on a chromosomes
3.2.S1: Use of databases to identify the focus of a human gene and its polypeptide product
3.1.A2: Comparison of the number of genes in humans with other species
3.1.S1: Use of a database to determine differences in the base sequence of a gene in two species
7.3.NOS: Developments in scientific research follow improvements in computing- the use of commuters has enabled scientists to make advances in bioinformatics applications such as locating genes within genomes and identifying conserved sequences
3.1.U3: The various specific forms of a gene are alleles
3.1.U4: Alleles differ from each other by one or only a few bases.
3.1.U5: New alleles are formed by mutation
3.1.A1: The causes of sickle cell anemia, including a base substitution mutation, a change to the base sequence of mRNA transcribed from it and a change to the sequence of a polypeptide in hemoglobin.
3.4.U10 Radiation and mutagenic chemicals increase the mutation rate and can cause genetic diseases and cancer.
3.4.A4 Consequences of radiation after nuclear bombing of Hiroshima and accident at Chernobyl.
3.1.U6: The genome is the whole of the genetic information of an organism
3.2.A2 Comparison of genome size in T2 phage, Escherichia coli, Drosophila melanogaster, Homo sapiens, Paris japonica.
3.1.U7: The entire base sequence of human genes was sequenced in the Human Genome Project
3.1.NOS: Developments in scientific research follow improvements in technology-gene sequencers are used for the sequencing of genes
7.1.A3: Use of nucleotides containing dideoxyribonucleic acid to stop DNA replication in preparation of samples for base sequencing
3.1.U1: A gene is a heritable factor that consists of a length of DNA and influences a specific characteristic
3.1.U2: A gene occupies a specific position on a chromosomes
3.2.S1: Use of databases to identify the focus of a human gene and its polypeptide product
3.1.A2: Comparison of the number of genes in humans with other species
3.1.S1: Use of a database to determine differences in the base sequence of a gene in two species
7.3.NOS: Developments in scientific research follow improvements in computing- the use of commuters has enabled scientists to make advances in bioinformatics applications such as locating genes within genomes and identifying conserved sequences
3.1.U3: The various specific forms of a gene are alleles
3.1.U4: Alleles differ from each other by one or only a few bases.
3.1.U5: New alleles are formed by mutation
3.1.A1: The causes of sickle cell anemia, including a base substitution mutation, a change to the base sequence of mRNA transcribed from it and a change to the sequence of a polypeptide in hemoglobin.
3.4.U10 Radiation and mutagenic chemicals increase the mutation rate and can cause genetic diseases and cancer.
3.4.A4 Consequences of radiation after nuclear bombing of Hiroshima and accident at Chernobyl.
3.1.U6: The genome is the whole of the genetic information of an organism
3.2.A2 Comparison of genome size in T2 phage, Escherichia coli, Drosophila melanogaster, Homo sapiens, Paris japonica.
3.1.U7: The entire base sequence of human genes was sequenced in the Human Genome Project
3.1.NOS: Developments in scientific research follow improvements in technology-gene sequencers are used for the sequencing of genes
7.1.A3: Use of nucleotides containing dideoxyribonucleic acid to stop DNA replication in preparation of samples for base sequencing
Genes ppt |
Genes quizlet |
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