Difference between revisions of "User talk:Kaznagul Sarkyt"
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You will probably want to read the [[Help:Contents|help pages]]. | You will probably want to read the [[Help:Contents|help pages]]. | ||
Again, welcome and have fun! [[User:S|S]] 23:44, 17 September 2016 (KST) | Again, welcome and have fun! [[User:S|S]] 23:44, 17 September 2016 (KST) | ||
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+ | == Essay: What is sequencing in Genomics and Omics? (as an approach of understanding life). Sequencing. == | ||
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+ | <p>Omics aims at the collective characterization and measurement of pools of biological molecules that interpret into the structure, function, and dynamics of living things. Genomics is the new science that deals with the discovery and taking notes of the considerable number of sequences in the whole genome of a specific living organism. The genome can be characterized as the complete arrangement of genes inside a cell. Genomics is, hence, the investigation of the genetic make-up of organisms.</p> | ||
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+ | <p>Genome sequencing is figuring out the order of DNA nucleotides, or bases, in a genome—the order of As, Cs, Gs, and Ts that make up a life form's DNA. The human genome is comprised of more than 3 billion of these genetic letters.</p> | ||
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+ | <p>Genome sequencing is frequently contrasted with "decoding," yet a sequence is still particularly in code. One might say, a genome sequence is just a long series of letters in a mysterious language.</p> | ||
+ | |||
+ | <p>When you read a sentence, the meaning is not simply in the arrangement of the letters. It is additionally in the words those letters make and in the sentence structure of the language. Thus, the human genome is more than simply its sequence. Imagine the genome as a book written without capitalization or punctuation, without breaks between words, sentences, or paragraphs, and with strings of nonsense letters scattered between and even inside sentences.</p> | ||
+ | |||
+ | <p>Sequencing the genome is a vital step towards understanding it. In any event, the genome succession will speak to a profitable easy route, helping researchers discover genes more effectively and faster. A genome arrangement contains a few signs about where genes are, despite the fact that researchers are simply figuring out how to decipher these pieces of information.</p> | ||
+ | |||
+ | <p>Scientists also hope that having the capacity to concentrate on the whole genome arrangement will help them see how the genome overall functions—how gene cooperate to coordinate the development, improvement and support of a whole organism.</p> | ||
+ | |||
+ | <p>Finally, genes account for less than 25 percent of the DNA in the genome, and so, I think, knowing the entire genome sequence will help scientists study the parts of the genome outside the genes. This includes the regulatory regions that control how genes are turned on an off, as well as long stretches of "nonsense" DNA—so called because we don't yet know what, if anything, it does.</p> | ||
+ | |||
+ | == What is BioRxiv? == | ||
+ | |||
+ | <p><strong>BioRxiv</strong> is a free online archive and distribution service for unpublished preprints in the life sciences. It is operated by Cold Spring Harbor Laboratory, a not-for-profit research and educational institution. By posting preprints on bioRxiv, authors are able to make their findings immediately available to the scientific community and receive feedback on draft manuscripts before they are submitted to journals.</p> | ||
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+ | <p> </p> | ||
+ | |||
+ | <p>1) All articles undergo a basic screening process for offensive and/or non-scientific content and are checked for plagiarism.</p> | ||
+ | |||
+ | <p>2) Authors may submit a revised version of an article to bioRxiv at any time. Once posted on bioRxiv, articles are citable and therefore cannot be removed.</p> | ||
+ | |||
+ | <p>3) Articles in the physical sciences, mathematics, or social sciences should only be posted on bioRxiv if they have direct relevance to the life sciences.</p> | ||
+ | |||
+ | <p>4) Articles in bioRxiv are categorized as New Results, Confirmatory Results, or Contradictory Results. New Results describe an advance in a field. Confirmatory Results largely replicate and confirm previously published work, whereas Contradictory Results largely replicate experimental approaches used in previously published work but the results contradict and/or do not support it.</p> | ||
+ | |||
+ | <p>5) Readers may add public comments to articles on bioRxiv. Comments are moderated to ensure they conform to the standards of normal professional discourse. Readers are also free to contact authors directly.</p> | ||
+ | |||
+ | <p> </p> | ||
+ | |||
+ | <p>In my opinion, BioRxiv is very useful and essential tool for most of the scientists, researchers, and students, who are in Life Sciences department. I learned about it and now I am highly motivated and inspired to use this website and enlarge my skills and horizons. I am looking forward learning more about Biology Science. </p> |
Latest revision as of 14:59, 2 October 2016
Welcome to Biolecture.org! We hope you will contribute much and well. You will probably want to read the help pages. Again, welcome and have fun! S 23:44, 17 September 2016 (KST)
Essay: What is sequencing in Genomics and Omics? (as an approach of understanding life). Sequencing.
Omics aims at the collective characterization and measurement of pools of biological molecules that interpret into the structure, function, and dynamics of living things. Genomics is the new science that deals with the discovery and taking notes of the considerable number of sequences in the whole genome of a specific living organism. The genome can be characterized as the complete arrangement of genes inside a cell. Genomics is, hence, the investigation of the genetic make-up of organisms.
Genome sequencing is figuring out the order of DNA nucleotides, or bases, in a genome—the order of As, Cs, Gs, and Ts that make up a life form's DNA. The human genome is comprised of more than 3 billion of these genetic letters.
Genome sequencing is frequently contrasted with "decoding," yet a sequence is still particularly in code. One might say, a genome sequence is just a long series of letters in a mysterious language.
When you read a sentence, the meaning is not simply in the arrangement of the letters. It is additionally in the words those letters make and in the sentence structure of the language. Thus, the human genome is more than simply its sequence. Imagine the genome as a book written without capitalization or punctuation, without breaks between words, sentences, or paragraphs, and with strings of nonsense letters scattered between and even inside sentences.
Sequencing the genome is a vital step towards understanding it. In any event, the genome succession will speak to a profitable easy route, helping researchers discover genes more effectively and faster. A genome arrangement contains a few signs about where genes are, despite the fact that researchers are simply figuring out how to decipher these pieces of information.
Scientists also hope that having the capacity to concentrate on the whole genome arrangement will help them see how the genome overall functions—how gene cooperate to coordinate the development, improvement and support of a whole organism.
Finally, genes account for less than 25 percent of the DNA in the genome, and so, I think, knowing the entire genome sequence will help scientists study the parts of the genome outside the genes. This includes the regulatory regions that control how genes are turned on an off, as well as long stretches of "nonsense" DNA—so called because we don't yet know what, if anything, it does.
What is BioRxiv?
BioRxiv is a free online archive and distribution service for unpublished preprints in the life sciences. It is operated by Cold Spring Harbor Laboratory, a not-for-profit research and educational institution. By posting preprints on bioRxiv, authors are able to make their findings immediately available to the scientific community and receive feedback on draft manuscripts before they are submitted to journals.
1) All articles undergo a basic screening process for offensive and/or non-scientific content and are checked for plagiarism.
2) Authors may submit a revised version of an article to bioRxiv at any time. Once posted on bioRxiv, articles are citable and therefore cannot be removed.
3) Articles in the physical sciences, mathematics, or social sciences should only be posted on bioRxiv if they have direct relevance to the life sciences.
4) Articles in bioRxiv are categorized as New Results, Confirmatory Results, or Contradictory Results. New Results describe an advance in a field. Confirmatory Results largely replicate and confirm previously published work, whereas Contradictory Results largely replicate experimental approaches used in previously published work but the results contradict and/or do not support it.
5) Readers may add public comments to articles on bioRxiv. Comments are moderated to ensure they conform to the standards of normal professional discourse. Readers are also free to contact authors directly.
In my opinion, BioRxiv is very useful and essential tool for most of the scientists, researchers, and students, who are in Life Sciences department. I learned about it and now I am highly motivated and inspired to use this website and enlarge my skills and horizons. I am looking forward learning more about Biology Science.