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Meaning · in Bombay, correct thing to do is :Q:

How to pass the file path as a parameter in ssis file output

I have a ssis package which have an output to file.
I have a environment variable name called @FolderLocation and I want to use this variable value in the parameter @Path.
I did this in the ssis file output/properties/Parameters/Parameters.
@Parameters
@{“Path” = “%_UserProfile%\Desktop\TTTTTTTT.txt”;
“FolderLocation” = “C:\Users\tss\Desktop”;}

I am getting an error that says

The variable “Path” is not declared.

Any help is appreciated.

A:

No. You cannot pass environment variables to file output. You need to use script task to do this. Note that the text between ; is a comment and it is ignored.
Create a new variable (in your case @FolderLocation) in the script task. Add the following script to the Script Task Editor.
@”%ProgramFiles%\Microsoft SQL Server\100\Tools\Binn\ScriptDom.exe” /language:C# /define:”System.String” /reference:”mscorlib.dll,System.Core.dll,System.Data.dll,System.Xml.dll,System.Xml.Linq.dll,System.Data.SqlClient.dll,System.Data.SqlTypes.dll,System.Data.SqlXml.dll”

function GetFileNameFromFolder(const FolderPath: String): String;
const
ExeName: String = ‘System.String’;
begin
Result := FolderPath;
if EndPath(Result) = ” then
begin
Result := TrimEnd(Result,”);
if Pos(”, Result) > 0 then
Result := Trim(Result, ”);
end;
end;

begin
Dts.Variables[‘User::FolderLocation’].Value := GetFileNameFromFolder(CurrentRow.FS);
end;

Then add this script task to the control flow of your package.

the number of most highly expressed genes for each

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The genetic diversity and evolution of the marine sponge Dysidea avara was studied using allozyme polymorphisms, with particular emphasis on the lectin-like Ca2+-dependent carbohydrate binding specificity of its fucose-specific lectin (avaricin). We analyzed a total of 129 cytosolic, 44 plasma membrane, and 13 sarcoplasmic reticulum fractions, which represent the different cellular compartments in this species. All samples were run on starch gels in two dimensions and resolved with silver staining. In total, 41 loci and 45 alleles were identified. Fifteen of these were polymorphic, making up 27% of the total number of loci investigated. We observed 16% of the total number of alleles in all subcellular fractions. The absence of avaricin in these fractions suggests that it is synthesized and secreted into the extra-cellular space. Within all three compartments, there was considerable population structure, as reflected by FST values, which were above the threshold level of 0.15. The data suggest that dysidein is the major genetic marker for this species. Avaricin differs from the other lectins described in the subphylum Choristida and is characterized by a lack of T-cell epitopes and a higher frequency of phenylalanine residues. Avaricin is the first lectin from a sponge to have amino acid sequence homology with Ca+2-dependent lectins from plant species.description>EnvInfo
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