<h2><strong>Writing genomic vocabulary in my definitions</strong> </h2>
<ol>
<li>Bioinformatics: Study for biology by using lots of information.</li>
<li>Genomics: Study for analyzing of DNA sequences</li>
<li>DNA: carries the genetic information, is consisted by bases and has double helix forms </li>
<li>RNA: has lost of forms to use DNA such as messenger, translation helper, and ribosome helper. </li>
<li>Allele: it’s component of chromosome. Two alleles usually form chromosome. </li>
<li>Alternative splicing: during transcription, exon is randomly chosen.</li>
<li>Base: is component of DNA and RNA. usually adenosine Thymine cytosine guanine are base</li>
<li>Sequencing: it’s order of things</li>
<li>Codon: three bases that consist a single amino acid</li>
<li>Copy number variant: 1000 base to 3M base pair are changed</li>
<li>Minor allele frequency: the allele which has less</li>
<li>Exome: exon sequencing</li>
<li>CG content: part where cytosine and guanine are abundant.</li>
<li>Inheritance: parent genic information goes to their offspring</li>
<li>Whole exome sequencing: reading the parts of every exomes</li>
<li>Phenotype: the expression that people can indicate</li>
<li>Genotype: gene information</li>
<li>Heterozygous: chromosome has different type of alleles</li>
<li>Homozygous: chromosome has same type of alleles</li>
<li>Hybridization: binding two objects</li>
<li>Locus: parts decided portion of chromosome</li>
<li>Methylation: methyl attaching</li>
<li>Mutation: is not normal by change</li>
<li>Missense Mutation: amino acid is changed by altering bases</li>
<li>Silence Mutation: no change but there is change in base</li>
<li>Oncogene: gene which is related to cancer</li>
<li>Polymorphism: which has more than one characters</li>
<li>Promotor: parts that transcription begun</li>
<li>Polymerase Chain Reaction: reaction to replicate object</li>
<li>Translocation: changing the location</li>
</ol>
