Single-cell RNA-sequencing (scRNA-seq) provides the chance to analyze heterogeneous cellular compositions and probe the patterns of gene expression that are unique to each cell type under various circumstances. However, batch effects like lab setups and individual variability make it difficult to use them in cross-condition designs.
<h3>What is Single-cell transcriptomes ?</h3>
In single-cell transcriptomics, the messenger RNA levels of hundreds to thousands of genes are simultaneously measured to assess the degree of gene expression in individual cells within a particular population.
<h3>Advantages : </h3>
• Integrated protocol proceeds directly from whole cells and preserves sample integrity.
• High resolution analysis enables discovery of cellular differences typically hidden by bulk sampling methods.
• Robust transcriptome analysis down to single-cell input levels for high-quality samples.
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The number of chromosomes does not correlate with the apparent complexity of an animal or a plant:
in humans, for example, the diploid number is 2n = 46 (that is, 23 pairs), compared with 2n = 78, or 39 pairs, in the dog and 2n = 36 (18) in the common earthworm.
Answer:
The evidence from the eruption helps scientists study past climate changes and compare them to modern changes.
Explanation:
Essentially, they like to study an area of difference so that they can see what changes in that situation; and they are able to understand <em>what </em> would change in a study sample (letting them know what measures to look for)
Answer:
25%
Explanation:
<em>The approximate proportion of G + C content in the genome of E. coli has been reported to be 50%. According to Chargaff's rule, the amount of guanine in any DNA must be approximately equal to the amount of cytosine. </em>Hence,
if G + C = 50 and G = C,
then
G = C = 25
Therefore, the approximate percentage of guanine in the genome of <em>E. coli </em>would be 25.
