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The software is very user-friendly and FAST! I have purchased several PDF software programs through the year and many times Nuance Scansoft PDF (ver. 2, 3, 4, 5, 6, 7) and have purchased the Foxit (Phantom PDF) one. I can say that the ease, the speediness of filling out PDF forms and its online platform make PDF Filler my number ONE PDF software now. I have only one recommendation. If you could make a tryout period available for the Professional and Business versions, that would be awesome!
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Mostly user friendly. Filling in multiple of the same form is not available, or finding that option is impossible. So I used same form over and over - using tab you also have to back space or use mouse to remove previous data and then fill in.
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2020-09-26
What do you like best? I love how I can neatly complete compliance filings that don't have a fillable PDF format using PDF filler. I can type on the form in PDF filler instead of having to print a hard copy and hand write or use a typewriter - who even has access to one of those anymore, lol? What do you dislike? It can be tricky to get the alignment just right and then save the completed document. Recommendations to others considering the product: Great tool for using to complete documents that don't have fillable format. What problems are you solving with the product? What benefits have you realized? Completing compliance filings for various States that don't offer fillable PDF forms.
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2020-08-31

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Copy Number Variants — Copy Number Variation. The gene copy number (also “copy number variants” or CNS) is the number of copies of a particular gene in the genotype of an individual. Recent evidence shows that the gene copy number can be elevated in cancer cells.
copy number. The number of copies of a particular PLASMID per CHROMOSOME present in a CELL. The number of copies of a GENE in the GENOME of an ORGANISM.
CNS are then detected based on the frequency of the reads (read depth) or aberrations in the mate pairs, after mapping the short reads to the reference genome. The majority of the current CNV detection tools analyze only one sample genome, at a time.
Plasmid copy number was determined by comparing the quantification signal from the plasmid to those from the chromosome. Copy number was then calculated by using a known copy number plasmid as a standard.
Refers to the genetic trait involving the number of copies of a particular gene present in the genome of an individual. Copy number variants account for a significant proportion of the genetic variation between individuals. Also called CNV.
The gene copy number (also “copy number variants” or CNS) is the number of copies of a particular gene in the genotype of an individual. Recent evidence shows that the gene copy number can be elevated in cancer cells. It was generally thought that genes were almost always present in two copies in a genome.
A copy number variation (CNV) is when the number of copies of a particular gene varies from one individual to the next. Following the completion of the Human Genome Project, it became apparent that the genome experiences gains and losses of genetic material.
Refers to the genetic trait involving the number of copies of a particular gene present in the genome of an individual. Genetic variants, including insertions, deletions, and duplications of segments of DNA, are also collectively referred to as copy number variants.

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